TY - GEN A1 - Weber, Marcus A1 - Meyer, Holger T1 - ZIBgridfree - Adaptive Conformation Analysis with qualified Support of Transition States and Thermodynamic Weights N2 - This paper introduces a new algorithm of conformational analysis based on mesh-free methods as described in [M. Weber. Mehless methods in Conformation Dynamics.(2005)]. The adaptive decomposition of the conformational space by softly limiting functions avoids trapping effects and allows adaptive refinement strategies. These properties of the algorithm makes ZIBgridfree particularly suitable for the complete exploration of high-dimensional conformational space. The adaptive control of the algorithm benefits from the tight integration of molecular simulation and conformational analysis. An emphasized part of the analysis is the Robust Perron Cluster Analysis (PCCA+) based on the work of Peter Deuflhard and Marcus Weber. PCCA+ supports an almost-characteristic cluster definition with an outstanding mapping of transition states. The outcome is expressed by the metastable sets of conformations, their thermodynamic weights and flexibility. T3 - ZIB-Report - 05-17 KW - Molecular Dynamics KW - Meshfree Methods KW - Conformation Analysis KW - Quality Functions Y1 - 2005 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:0297-zib-8514 ER - TY - GEN A1 - Weber, Marcus A1 - Galliat, Tobias T1 - Characterization of Transition States in Conformational Dynamics using Fuzzy Sets N2 - Recently, a novel approach for the analysis of molecular dynamics on the basis of a transfer operator has been introduced. Therein conformations are considered to be disjoint metastable clusters within position space of a molecule. These clusters are defined by almost invariant characteristic functions that can be computed via {\em Perron Cluster} analysis. The present paper suggests to replace crisp clusters with {\em fuzzy} clusters, i.e. to replace characteristic functions with membership functions. This allows a more sufficient characterization of transiton states between different confor conformations and therefore leads to a better understanding of molecular dynamics. Fur thermore, an indicator for the uniqueness of metastable fuzzy clusters and a fast algorithm for the computation of these clusters are described. Numerical examples are included. T3 - ZIB-Report - 02-12 KW - biochemical conformations KW - conformational dynamics KW - molecular dynamics KW - cluster analysis KW - transition states KW - fuzzy sets Y1 - 2002 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:0297-zib-6791 ER - TY - GEN A1 - Cordes, Frank A1 - Weber, Marcus A1 - Schmidt-Ehrenberg, Johannes T1 - Metastable Conformations via successive Perron-Cluster Cluster Analysis of dihedrals N2 - Decomposition of the high dimensional conformational space of bio-molecules into metastable subsets is used for data reduction of long molecular trajectories in order to facilitate chemical analysis and to improve convergence of simulations within these subsets. The metastability is identified by the Perron-cluster cluster analysis of a Markov process that generates the thermodynamic distribution. A necessary prerequisite of this analysis is the discretization of the conformational space. A combinatorial approach via discretization of each degree of freedom will end in the so called ''curse of dimension''. In the following paper we analyze Hybrid Monte Carlo simulations of small, drug-like biomolecules and focus on the dihedral degrees of freedom as indicators of conformational changes. To avoid the ''curse of dimension'', the projection of the underlying Markov operator on each dihedral is analyzed according to its metastability. In each decomposition step of a recursive procedure, those significant dihedrals, which indicate high metastability, are used for further decomposition. The procedure is introduced as part of a hierarchical protocol of simulations at different temperatures. The convergence of simulations within metastable subsets is used as an ''a posteriori'' criterion for a successful identification of metastability. All results are presented with the visualization program AmiraMol. T3 - ZIB-Report - 02-40 KW - metastability KW - Perron-Cluster Cluster Analysis KW - curse of dimension KW - Hybrid Monte Carlo KW - significant dihedrals Y1 - 2002 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:0297-zib-7074 ER - TY - GEN A1 - Kube, Susanna A1 - Weber, Marcus T1 - Conformation Kinetics as a Reduced Model for Transition Pathways N2 - The complexity of molecular kinetics can be reduced significantly by a restriction to metastable conformations which are almost invariant sets of molecular dynamical systems. With the Robust Perron Cl uster Analysis PCCA+, developed by Weber and Deuflhard, we have a tool available which can be used to identify these conformations from a transition probability matrix. This method can also be applied to the corresponding transition rate matrix which provides important information concerning transition pathways of single molecules. In the present paper, we explain the relationship between these tw o concepts and the extraction of conformation kinetics from transition rates. Moreover, we show how transition rates can be approximated and conclude with numerical examples. T3 - ZIB-Report - 05-43 KW - conformation kinetics KW - transition rates KW - Robust Perron Cluster Analysis Y1 - 2005 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:0297-zib-8763 ER - TY - GEN A1 - Weber, Marcus A1 - Rungsarityotin, Wasinee A1 - Schliep, Alexander T1 - Perron Cluster Analysis and Its Connection to Graph Partitioning for Noisy Data N2 - The problem of clustering data can be formulated as a graph partitioning problem. Spectral methods for obtaining optimal solutions have reveceived a lot of attention recently. We describe Perron Cluster Cluster Analysis (PCCA) and, for the first time, establish a connection to spectral graph partitioning. We show that in our approach a clustering can be efficiently computed using a simple linear map of the eigenvector data. To deal with the prevalent problem of noisy and possibly overlapping data we introduce the min Chi indicator which helps in selecting the number of clusters and confirming the existence of a partition of the data. This gives a non-probabilistic alternative to statistical mixture-models. We close with showing favorable results on the analysis of gene expressi on data for two different cancer types. T3 - ZIB-Report - 04-39 KW - Perron cluster analysis KW - spectral graph theory KW - clustering KW - gene expression Y1 - 2004 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:0297-zib-8140 ER - TY - GEN A1 - Weber, Marcus T1 - Improved Perron Cluster Analysis N2 - The problem of clustering data can often be transformed into the problem of finding a hidden block diagonal structure in a stochastic matrix. Deuflhard et al. have proposed an algorithm that state s the number $k$ of clusters and uses the sign structure of $k$ eigenvectors of the stochastic matrix to solve the cluster problem. Recently Weber and Galliat discovered that this system of eigenvectors can easily be transformed into a system of $k$ membership functions or soft characteristic functions describing the clusters. In this article we explain the corresponding cluster algorithm and point out the underlying theory. By means of numerical examples we explain how the grade of membership can be interpreted. T3 - ZIB-Report - 03-04 KW - cluster analysis KW - stochastic matrices KW - almost invariant sets Y1 - 2003 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:0297-zib-7260 ER - TY - GEN A1 - Deuflhard, Peter A1 - Weber, Marcus T1 - Robust Perron Cluster Analysis in Conformation Dynamics N2 - The key to molecular conformation dynamics is the direct identification of metastable conformations, which are almost invariant sets of molecular dynamical systems. Once some reversible Markov operator has been discretized, a generalized symmetric stochastic matrix arises. This matrix can be treated by Perron cluster analysis, a rather recent method involving a Perron cluster eigenproblem. The paper presents an improved Perron cluster analysis algorithm, which is more robust than earlier suggestions. Numerical examples are included. T3 - ZIB-Report - 03-19 KW - Markov chains KW - cluster algorithms KW - Perron cluster analysis KW - conformation dynamics Y1 - 2003 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:0297-zib-7415 ER - TY - GEN A1 - Weber, Marcus T1 - Clustering by using a simplex structure N2 - In this paper we interpret clustering as a mapping of data into a simplex. If the data itself has simplicial struture this mapping becomes linear. Spectral analysis is an often used tool for clustering data. We will show that corresponding singular vectors or eigenvectors comprise simplicial structure. Therefore they lead to a cluster algorithm, which consists of a simple linear mapping. An example for this kind of algorithms is the Perron cluster analysis (PCCA). We have applied it in practice to identify metastable sets of molecular dynamical systems. In contrast to other algorithms, this kind of approach provides an a priori criterion to determine the number of clusters. In this paper we extend the ideas to more general problems like clustering of bipartite graphs. T3 - ZIB-Report - 04-03 KW - cluster algorithms KW - Perron cluster analysis KW - stochastic matrices KW - bipartite graphs Y1 - 2003 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:0297-zib-7782 ER - TY - GEN A1 - Weber, Marcus T1 - A Subspace Approach to Molecular Markov State Models via an Infinitesimal Generator N2 - Supercomputers can simulate complex molecular systems. However, there is a very large gap between the fastest oscillations of covalent bonds of a molecule and the time-scale of the dominant processes. In order to extract the dominant time-scales and to identify the dominant processes, a clustering of information is needed. This thesis shows that only the subspace-based Robust Perron Cluster Analysis (PCCA+) can solve this problem correctly by the construction of a Markov State Model. PCCA+ allows for time-extrapolation in molecular kinetics. This thesis shows the difference between molecular dynamics and molecular kinetics. Only in the molecular kinetics framework a definition of transition rates is possible. In this context, the existence of an infinitesimal generator of the dynamical processes is discussed. If the existence is assumed, the Theorem of Gauß can be applied in order to compute transition rates efficiently. Molecular dynamics, however, is not able to provide a suitable statistical basis for the determination of the transition pattern. T3 - ZIB-Report - 09-27 KW - Robuste Perron Cluster Analyse KW - Molekülkinetik KW - Übergangsraten KW - Robust Perron cluster analysis KW - molecular kinetics KW - transition rates Y1 - 2009 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:0297-zib-11432 SN - 1438-0064 ER - TY - GEN A1 - Weber, Marcus T1 - An efficient analysis of rare events in canonical ensemble dynamics N2 - For an analysis of a molecular system from a computational statistical thermodynamics point of view, extensive molecular dynamics simulations are very inefficient. During this procedure, at lot of redundant data is generated. Whereas the algorithms spend most of the computing time for a sampling of configurations within the basins of the potential energy landscape of the molecular system, the important information about the long-time behaviour of the molecules is given by transition regions and barriers between the basins, which are sampled rarely only. Thinking of molecular dynamics trajectories, researchers try to figure out which kind of dynamical model is suitable for an efficient simulation. This article suggests to change the point of view from extensive simulation of molecular dynamics trajectories to more efficient sampling strategies of the conformation dynamics approach. T3 - ZIB-Report - 08-36 KW - Moleküldynamik KW - Kanonische Gesamtheit KW - Metastabilität KW - molecular dynamics KW - canonical ensemble KW - metastability Y1 - 2008 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:0297-zib-10871 SN - 1438-0064 ER - TY - GEN A1 - Meyer, Holger A1 - Moll, Sebastian A1 - Cordes, Frank A1 - Weber, Marcus T1 - ConFlow? A new space-based Application for complete Conformational Analysis of Molecules N2 - Biochemical interactions are determined by the 3D-structure of the involved components - thus the identification of conformations is a key for many applications in rational drug design. {\sf ConFlow} is a new multilevel approach to conformational analysis with main focus on completeness in investigation of conformational space. In contrast to known conformational analysis, the starting point for design is a space-based description of conformational areas. A tight integration of sampling and analysis leads to an identification of conformational areas simultaneously during sampling. An incremental decomposition of high-dimensional conformational space is used to guide the analysis. A new concept for the description of conformations and their path connected components based on convex hulls and {\em Hypercubes}is developed. The first results of the {\sf ConFlow} application constitute a 'proof of concept' and are further more highly encouraging. In comparison to conventional industrial applications, {\sf ConFlow} achieves higher accuracy and a specified degree of completeness with comparable effort. T3 - ZIB-Report - 06-31 KW - conformational-analysis in-silico-screening drug-design Y1 - 2006 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:0297-zib-9258 ER - TY - GEN A1 - Kube, Susanna A1 - Weber, Marcus T1 - Coarse Grained Molecular Kinetics N2 - The dynamic behavior of molecules can often be described by Markov processes. From computational molecular simulations one can derive transition rates or transition probabilities between subsets of the discretized conformational space. On the basis of this dynamic information, the spatial subsets are combined into a small number of so-called metastable molecular conformations. This is done by clustering methods like the Robust Perron Cluster Analysis (PCCA+). Up to now it is an open question how this coarse graining in space can be transformed to a coarse graining of the Markov chain while preserving the essential dynamic information. In the following article we aim at a consistent coarse graining of transition probabilities or rates on the basis of metastable conformations such that important physical and mathematical relations are preserved. This approach is new because PCCA+ computes molecular conformations as linear combinations of the dominant eigenvectors of the transition matrix which does not hold for other clustering methods. T3 - ZIB-Report - 06-35 Y1 - 2006 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:0297-zib-9299 ER - TY - GEN A1 - Kube, Susanna A1 - Lasser, Caroline A1 - Weber, Marcus T1 - Monte Carlo sampling of Wigner functions and surface hopping quantum dynamics N2 - Wigner transformation provides a one-to-one correspondence between functions on position space (wave functions) and functions on phase space (Wigner functions). Weighted integrals of Wigner functions yield quadratic quantities of wave functions like position and momentum densities or expectation values. For molecular quantum systems, suitably modified classical transport of Wigner functions provides an asymptotic approximation of the dynamics in the high energy regime. The article addresses the computation of Wigner functions by Monte Carlo quadrature. An ad aption of the Metropolis algorithm for the approximation of signed measures with disconnected support is systematically tested in combination with a surface hopping algorithm for non-adiabatic quantum dynamics. The numerical experiments give expectation values and level populations with an error of two to three percent, which agrees with the theoretically expected accuracy. T3 - ZIB-Report - 07-17 KW - Metropolis Monte Carlo KW - approximation KW - quadrature KW - oscillating functions Y1 - 2007 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:0297-zib-9604 ER - TY - GEN A1 - Weber, Marcus A1 - Walter, Lionel A1 - Kube, Susanna A1 - Deuflhard, Peter T1 - Stable computation of probability densities for metastable dynamical systems N2 - Whenever the invariant stationary density of metastable dynamical systems decomposes into almost invariant partial densities, its computation as eigenvector of some transition probability matrix is an ill-conditioned problem. In order to avoid this computational difficulty, we suggest to apply an aggregation/disaggregation method which only addresses wellconditioned sub-problems and thus results in a stable algorithm. In contrast to existing methods, the aggregation step is done via a sampling algorithm which covers only small patches of the sampling space. Finally, the theoretical analysis is illustrated by two biomolecular examples. T3 - ZIB-Report - 06-39 KW - dynamical systems KW - metastability KW - molecular conformations KW - cluster analysis KW - sampling KW - aggregation/disaggregation KW - domain decomposition Y1 - 2006 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:0297-zib-9331 ER - TY - GEN A1 - Kube, Susanna A1 - Weber, Marcus T1 - Identification of Metastabilities in Monomolecular Conformation Kinetics N2 - The identification of metastable conformations of molecules plays an important role in computational drug design. One main difficulty is the fact that the underlying dynamic processes take place in high dimensional spaces. Although the restriction of degrees of freedom to a few dihedral angles significantly reduces the complexity of the problem, the existing algorithms are time-consuming. They are based on the approximation of transition probabilities by an extensive sampling of states according to the Boltzmann distribution. We present a method which can identify metastable conformations without sampling the complete distribution. Our algorithm is based on local transition rates and uses only pointwise information about the potential energy surface. In order to apply the cluster algorithm PCCA+, we compute a few eigenvectors of the rate matrix by the Jacobi-Davidson method. Interpolation techniques are applied to approximate the thermodynamical weights of the clusters. The concluding example illustrates our approach for epigallocatechine, a molecule which can be described by seven dihedral angles. T3 - ZIB-Report - 06-01 KW - metastable conformations KW - potential energy surface KW - transition rates KW - eigenvectors KW - clustering Y1 - 2005 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:0297-zib-8956 ER - TY - GEN A1 - Weber, Marcus A1 - Kube, Susanna A1 - Riemer, Alexander A1 - Bujotzek, Alexander T1 - Efficient Sampling of the Stationary Distribution of Metastable Dynamical Systems N2 - In this article we aim at an efficient sampling of the stationary distribution of dynamical systems in the presence of metastabilities. In the past decade many sophisticated algorithms have been inven ted in this field. We do not want to simply add a further one. We address the problem that one has applied a sampling algorithm for a dynamical system many times. This leads to different samplings which more or less represent the stationary distribution partially very well, but which are still far away from ergodicity or from the global stationary distribution. We will show how these samplings can be joined together in order to get one global sampling of the stationary distribution. T3 - ZIB-Report - 07-03 KW - dynamical systems KW - stationary distribution KW - rare events KW - metastability KW - cluster analysis Y1 - 2006 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:0297-zib-9467 ER - TY - GEN A1 - Walter, Lionel A1 - Weber, Marcus T1 - ConfJump : a fast biomolecular sampling method which drills tunnels through high mountains N2 - In order to compute the thermodynamic weights of the different metastable conformations of a molecule, we want to approximate the molecule's Boltzmann distribution in a reasonable time. This is an essential issue in computational drug design. The energy landscape of active biomolecules is generally very rough with a lot of high barriers and low regions. Many of the algorithms that perform such samplings (e.g. the hybrid Monte Carlo method) have difficulties with such landscapes. They are trapped in low-energy regions for a very long time and cannot overcome high barriers. Moving from one low-energy region to another is a very rare event. For these reasons, the distribution of the generated sampling points converges very slowly against the thermodynamically correct distribution of the molecule. The idea of ConfJump is to use $a~priori$ knowledge of the localization of low-energy regions to enhance the sampling with artificial jumps between these low-energy regions. The artificial jumps are combined with the hybrid Monte Carlo method. This allows the computation of some dynamical properties of the molecule. In ConfJump, the detailed balance condition is satisfied and the mathematically correct molecular distribution is sampled. T3 - ZIB-Report - 06-26 KW - Monte Carlo simulation KW - rare events KW - rough potential energy function KW - molecular dynamics Y1 - 2006 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:0297-zib-9204 ER - TY - THES A1 - Weber, Marcus T1 - Meshless Methods in Confirmation Dynamics Y1 - 2006 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:0297-zib-10232 ER - TY - GEN A1 - Weber, Marcus A1 - Becker, Roland A1 - Köppen, Robert A1 - Durmaz, Vedat T1 - Classical hybrid Monte-Carlo simulations of the interconversion of hexabromocyclododecane N2 - In this paper, we investigate the interconversion processes of the major flame retardant -- 1,2,5,6,9,10-hexabromocyclododecane (HBCD) -- by the means of statistical thermodynamics based on classical force-fields. Three ideas will be presented. First, the application of classical hybrid Monte-Carlo simulations for quantum mechanical processes will be justified. Second, the problem of insufficient convergence properties of hybrid Monte-Carlo methods for the generation of low temperature canonical ensembles will be solved by an interpolation approach. Furthermore, it will be shown how free energy differences can be used for a rate matrix computation. The results of our numerical simulations will be compared to experimental results. T3 - ZIB-Report - 07-31 KW - Markov process KW - molecular dynamics KW - rate matrix Y1 - 2007 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:0297-zib-10308 SN - 1438-0064 ER - TY - GEN A1 - Weber, Marcus T1 - Conformation-based transition state theory N2 - For the treatment of equilibrated molecular systems in a heat bath we propose a transition state theory that is based on conformation dynamics. In general, a set-based discretization of a Markov operator ${\cal P}^\tau$ does not preserve the Markov property. In this article, we propose a discretization method which is based on a Galerkin approach. This discretization method preserves the Markov property of the operator and can be interpreted as a decomposition of the state space into (fuzzy) sets. The conformation-based transition state theory presented here can be seen as a first step in conformation dynamics towards the computation of essential dynamical properties of molecular systems without time-consuming molecular dynamics simulations. T3 - ZIB-Report - 07-18 KW - dynamical systems KW - transition state theory KW - rare events Y1 - 2007 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:0297-zib-9612 ER - TY - GEN A1 - Weber, Marcus T1 - The funnel trap paradox N2 - In this article, an illustrative example is given for the coarse-graining of a Markov process which leads to a shift in the statistical weights of a two-states-system. The example is based on a 2D-funnel trap. The funnel trap is constructed in such a way, that the area inside and outside of the trap is identical. However, observing the flight of the insect as a Markov process, the probability for being “in the trap” is higher. This example can be transferred to several kinds of processes (like receptor-ligandbinding processes in chemistry) and describes the influence of “re-entering events”. T3 - ZIB-Report - 12-12 KW - Markov process KW - Robust Perron Cluster Analysis KW - Conformation Dynamics Y1 - 2012 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:0297-zib-14765 SN - 1438-0064 ER - TY - JOUR A1 - Abendroth, Frank A1 - Bujotzek, Alexander A1 - Shan, Min A1 - Haag, Rainer A1 - Weber, Marcus A1 - Seitz, Oliver T1 - DNA-controlled bivalent presentation of ligands for the estrogen receptor JF - Angew. Chem. Int. Ed. Y1 - 2011 ER - TY - THES A1 - Weber, Marcus T1 - A Subspace Approach to Molecular Markov State Models via a New Infinitesimal Generator N2 - Supercomputers can simulate complex molecular systems. However, there is a very large gap between the fastest oscillations of covalent bonds of a molecule and the time-scale of the dominant processes. In order to extract the dominant time-scales and to identify the dominant processes, a clustering of information is needed. This thesis shows that only the subspace-based Robust Perron Cluster Analysis (PCCA+) can solve this problem correctly by the construction of a Markov State Model. PCCA+ allows for time-extrapolation in molecular kinetics. This thesis shows the difference between molecular dynamics and molecular kinetics. Only in the molecular kinetics framework a definition of transition rates is possible. In this context, the existence of an infinitesimal generator of the dynamical processes is discussed. If the existence is assumed, the Theorem of Gauß can be applied in order to compute transition rates efficiently. Molecular dynamics, however, is not able to provide a suitable statistical basis for the determination of the transition pattern. KW - Conformation Dynamics KW - Molecular Kinetics KW - Transition Rates KW - Markov State Models Y1 - 2011 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:0297-zib-14025 ER - TY - JOUR A1 - Bujotzek, Alexander A1 - Shan, Min A1 - Haag, Rainer A1 - Weber, Marcus T1 - Towards a rational spacer design for bivalent inhibition of estrogen receptor JF - J. Comput.-Aided Mol. Des. Y1 - 2011 VL - 25(3) SP - 253 EP - 262 ER - TY - CHAP A1 - Deuflhard, Peter A1 - Weber, Marcus T1 - Robust Perron Cluster Analysis in Conformation Dynamics T2 - Lin. Alg. Appl. – Special Issue on Matrices and Mathematical Biology Y1 - 2005 VL - 398 SP - 161 EP - 184 PB - Elsevier Journals CY - Germany ER - TY - JOUR A1 - Haack, Fiete A1 - Röblitz, Susanna A1 - Scharkoi, Olga A1 - Schmidt, Burkhard A1 - Weber, Marcus T1 - Adaptive Spectral Clustering for Conformation Analysis JF - AIP Conference Proceedings Y1 - 2010 UR - http://link.aip.org/link/?APC/1281/1585/1 U6 - https://doi.org/10.1063/1.3498116 VL - 1281 IS - 1 SP - 1585 EP - 1588 PB - AIP ER - TY - CHAP A1 - Kube, Susanna A1 - Weber, Marcus T1 - Computation of equilibrium densities in metastable dynamical systems by domain decomposition T2 - Numerical Analysis and Applied Mathematics, International Conference on Numerical Analysis and Applied Mathematics 2008 Y1 - 2008 VL - 1048 SP - 339 EP - 342 PB - AIP Conference Proceedings ER - TY - JOUR A1 - Kube, Susanna A1 - Weber, Marcus T1 - A Coarse Graining Method for the Identification of Transition rates between Molecular Conformations JF - Journal of Chemical Physics Y1 - 2007 U6 - https://doi.org/10.1063/1.2404953 VL - 126 IS - 2 ER - TY - JOUR A1 - Metzner, Ph. A1 - Weber, Marcus A1 - Schütte, Christof T1 - Observation uncertainty in reversible Markov chains JF - Phys. Rev. E Y1 - 2010 U6 - https://doi.org/10.1103/PhysRevE.82.031114 VL - 82 IS - 3 SP - 031114 PB - American Physical Society ER - TY - JOUR A1 - Gürler, A. A1 - Moll, Sebastian A1 - Weber, Marcus A1 - Meyer, Holger A1 - Cordes, Frank T1 - Selection and flexible optimization of binding modes from conformation ensembles JF - Biosystems Y1 - 2007 ER - TY - JOUR A1 - Guerler, A. A1 - Moll, Sebastian A1 - Weber, Marcus A1 - Meyer, Holger A1 - Cordes, Frank T1 - Selection and flexible optimization of binding modes from conformation ensembles JF - Biosystems Y1 - 2008 UR - http://www.sciencedirect.com/science/article/pii/S0303264707001670 U6 - https://doi.org/DOI: 10.1016/j.biosystems.2007.11.004 VL - 92 IS - 1 SP - 42 EP - 48 ER - TY - CHAP A1 - Weber, Marcus A1 - Kube, Susanna T1 - Robust Perron Cluster Analysis for Various Applications in Computational Life Science T2 - Computational Life Sciences Y1 - 2005 SP - 57 EP - 66 ER - TY - JOUR A1 - Klimm, Martina A1 - Bujotzek, Alexander A1 - Weber, Marcus T1 - Direct Reweighting Strategies in Conformation Dynamics JF - MATCH Commun. Math. Comp. Chem. Y1 - 2011 VL - 65(2) SP - 333 EP - 346 ER - TY - JOUR A1 - Durmaz, Vedat A1 - Weber, Marcus A1 - Becker, Roland T1 - How to Simulate Affinities for Host-Guest Systems Lacking Binding Mode Information: application to the liquid chromatographic separation of hexabromocyclododecane stereoisomers JF - Journal of Molecular Modeling Y1 - 2012 U6 - https://doi.org/10.1007/s00894-011-1239-5 VL - 18 SP - 2399 EP - 2408 ER - TY - JOUR A1 - Weber, Marcus A1 - Bujotzek, Alexander A1 - Haag, Rainer T1 - Quantifying the rebinding effect in multivalent chemical ligand-receptor systems JF - J. Chem. Phys. Y1 - 2012 VL - 137 IS - 5 SP - 054111 ER - TY - JOUR A1 - Fasting, Carlo A1 - Schalley, Christoph A. A1 - Weber, Marcus A1 - Seitz, Oliver A1 - Hecht, Stefan A1 - Koksch, Beate A1 - Dernedde, Jens A1 - Graf, Christina A1 - Knapp, Ernst-Walter A1 - Haag, Rainer T1 - Multivalency as a Chemical Organization and Action Principle JF - Angew. Chem. Int. Ed. Y1 - 2012 VL - 51 IS - 42 SP - 10472 EP - 10498 ER - TY - JOUR A1 - Köppen, Robert A1 - Riedel, Juliane A1 - Proske, Matthias A1 - Drzymala, Sarah A1 - Rasenko, Tatjana A1 - Durmaz, Vedat A1 - Weber, Marcus A1 - Koch, Matthias T1 - Photochemical trans-/cis-isomerization and quantification of zearalenone in edible oils JF - J. Agric. Food Chem. Y1 - 2012 U6 - https://doi.org/10.1021/jf3037775 VL - 60 SP - 11733 EP - 11740 ER - TY - JOUR A1 - Kube, Susanna A1 - Lasser, Caroline A1 - Weber, Marcus T1 - Monte Carlo sampling of Wigner functions and surface hopping quantum dynamics JF - Journal of Computational Physics Y1 - 2008 U6 - https://doi.org/10.1016/j.jcp.2008.11.016 VL - 228 IS - 6 SP - 1947 EP - 1962 ER - TY - GEN A1 - Kellermann, R. A1 - Weber, Marcus A1 - Bujotzek, Alexander T1 - Vom Dietrich zum Sicherheitsschlüssel – Mathematiker des Matheon simulieren neuen Wirkstoff für die Diabetes-Behandlung Y1 - 2007 IS - 2 PB - DFG-Forschungszentrum Matheon ER - TY - JOUR A1 - Köppen, Robert A1 - Becker, Roland A1 - Weber, Marcus A1 - Durmaz, Vedat A1 - Nehls, Irene T1 - HBCD stereoisimers: Thermal interconversion and enantiospecific trace analysis in biota JF - Organohalogen Compounds Y1 - 2009 VL - 70 SP - 910 EP - 913 ER - TY - JOUR A1 - Bujotzek, Alexander A1 - Weber, Marcus T1 - Efficient Simulation of Ligand-Receptor Binding Processes Using the Conformation Dynamics Approach JF - Journal of Bioinformatics and Computational Biology Y1 - 2009 VL - 7(5) SP - 811 EP - 831 ER - TY - CHAP A1 - Weber, Marcus ED - Dunemann, L. ED - Schmoll, O. T1 - Spurenstoffe im Trinkwasser - Risikoqualifizierung im Rechner? T2 - Schriftenreihe des Vereins für Wasser-, Boden- und Lufthygiene Y1 - 2009 ER - TY - JOUR A1 - Weber, Marcus A1 - Durmaz, Vedat A1 - Becker, Roland A1 - Esslinger, Susanne T1 - Predictive Identification of Pentabromocyclododecane (PBCD) Isomers with high Binding Affinity to hTTR JF - Organohalogen Compounds Y1 - 2009 VL - 71 SP - 247 EP - 252 ER - TY - JOUR A1 - Schütte, Christof A1 - Nielsen, Adam A1 - Weber, Marcus T1 - Markov State Models and Molecular Alchemy JF - Molecular Physics N2 - In recent years Markov State Models (MSMs) have attracted a consid- erable amount of attention with regard to modelling conformation changes and associated function of biomolecular systems. They have been used successfully, e.g., for peptides including time-resolved spectroscopic experiments, protein function and protein folding , DNA and RNA, and ligand-receptor interaction in drug design and more complicated multivalent scenarios. In this article a novel reweighting scheme is introduced that allows to construct an MSM for certain molecular system out of an MSM for a similar system. This permits studying how molecular properties on long timescales differ between similar molecular systems without performing full molecular dynamics simulations for each system under con- sideration. The performance of the reweighting scheme is illustrated for simple test cases including one where the main wells of the respective energy landscapes are located differently and an alchemical transformation of butane to pentane where the dimension of the state space is changed. KW - MSM KW - Reweighting KW - Girsanov Y1 - 2015 U6 - https://doi.org/10.1080/00268976.2014.944597 VL - 113 IS - 1 SP - 69 EP - 78 ER - TY - GEN A1 - Stein, Christoph A1 - Weber, Marcus A1 - Zöllner, Christian A1 - Scharkoi, Olga T1 - Fentanyl derivatives as pH-dependent opioid receptor agonists T2 - European Patent Application, Bulletin 2013/08 Y1 - 2013 ER - TY - GEN A1 - Stein, Christoph A1 - Weber, Marcus A1 - Scharkoi, Olga A1 - Deuflhard, Peter T1 - Method and system for identifying compounds that bind and preferably activate a target opioid receptor in a pH-dependent manner T2 - European Patent Application, Bulletin 2013/28 Y1 - 2013 ER - TY - GEN A1 - Schütte, Christof A1 - Nielsen, Adam A1 - Weber, Marcus T1 - Markov State Models and Molecular Alchemy N2 - In recent years Markov State Models (MSMs) have attracted a consid- erable amount of attention with regard to modelling conformation changes and associated function of biomolecular systems. They have been used successfully, e.g., for peptides including time-resolved spectroscopic ex- periments, protein function and protein folding , DNA and RNA, and ligand-receptor interaction in drug design and more complicated multi- valent scenarios. In this article a novel reweighting scheme is introduced that allows to construct an MSM for certain molecular system out of an MSM for a similar system. This permits studying how molecular proper- ties on long timescales differ between similar molecular systems without performing full molecular dynamics simulations for each system under con- sideration. The performance of the reweighting scheme is illustrated for simple test cases including one where the main wells of the respective en- ergy landscapes are located differently and an alchemical transformation of butane to pentane where the dimension of the state space is changed. T3 - ZIB-Report - 14-05 KW - Girsanov Theorem KW - Stochastic Differential Equation KW - Importance Sampling Y1 - 2014 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:0297-zib-46718 SN - 1438-0064 ER - TY - JOUR A1 - Shan, Min A1 - Carlson, Kathryn E. A1 - Bujotzek, Alexander A1 - Wellner, Anja A1 - Gust, Ronald A1 - Weber, Marcus A1 - Katzenellenbogen, John A. A1 - Haag, Rainer T1 - Nonsteroidal Bivalent Estrogen Ligands - An Application of the Bivalent Concept to the Estrogen Receptor JF - ACS Chem. Biol. Y1 - 2013 VL - 8 IS - 4 SP - 707 EP - 715 ER - TY - JOUR A1 - Weber, Marcus T1 - Adaptive Spectral Clustering in Molecular Simulation. In: Studies in Classification, Data Analysis, and Knowledge Organization JF - XIV: Classification and Data Mining, A. Giusti, G. Ritter, M. Vichi (Eds.), Springer Series Y1 - 2013 SP - 147 EP - 157 ER - TY - JOUR A1 - Shan, Min A1 - Bujotzek, Alexander A1 - Abendroth, Frank A1 - Seitz, Oliver A1 - Weber, Marcus A1 - Haag, Rainer T1 - Conformational Analysis of Bivalent Estrogen Receptor-Ligands: From Intramolecular to Intermolecular Binding JF - ChemBioChem, 12(17) Y1 - 2011 U6 - https://doi.org/10.1002/cbic.201100529 SP - 2587 EP - 2598 ER - TY - JOUR A1 - Scharkoi, Olga A1 - Esslinger, Susanne A1 - Becker, Roland A1 - Weber, Marcus A1 - Nehls, Irene T1 - Predicting sites of cytochrome P450-mediated hydroxylation applied to CYP3A4 and hexabromocyclododecane JF - Molecular Simulation Y1 - 2014 U6 - https://doi.org/10.1080/08927022.2014.898845 ER - TY - JOUR A1 - Scharkoi, O. A1 - Esslinger, Susanne A1 - Becker, Roland A1 - Weber, Marcus A1 - Nehls, Irene T1 - Phase I oxidation of alpha- and gamma-hexabromocyclododecane by cytochrome P450 enzymes: simulation of the stereoisomerism of hydroxylated metabolites JF - Organohalogen Compounds Y1 - 2011 VL - 73 SP - 730 EP - 733 ER - TY - JOUR A1 - Durmaz, Vedat A1 - Schmidt, Sebastian A1 - Sabri, Peggy A1 - Piechotta, Christian A1 - Weber, Marcus T1 - A hands-off linear interaction energy approach to binding mode and affinity estimation of estrogens JF - Journal of Chemical Information and Modeling Y1 - 2013 VL - 53 IS - 10 SP - 2681 EP - 2688 ER - TY - JOUR A1 - Tyagi, Rahul A1 - Malhotra, Shashwat A1 - Thünemann, Andreas F. A1 - Sedighi, Amir A1 - Weber, Marcus A1 - Schäfer, Andreas A1 - Haag, Rainer T1 - Investigations of Host-Guest Interactions with Shape-persistent Nonionic Dendritic Micelles JF - J. Phys. Chem. C Y1 - 2013 VL - 117 IS - 23 SP - 12307 EP - 12317 ER - TY - JOUR A1 - Weber, Marcus A1 - Zoschke, Christian A1 - Sedighi, Amir A1 - Fleige, Emanuel A1 - Haag, Rainer A1 - Schäfer-Korting, Monika T1 - Free Energy Simulations of Drug loading for Core-Multishell Nanotransporters JF - J Nanomed Nanotechnol Y1 - 2014 U6 - https://doi.org/10.4172/2157-7439.1000234 VL - 5 IS - 5 SP - 234 ER - TY - JOUR A1 - Djurdjevac Conrad, Natasa A1 - Weber, Marcus A1 - Schütte, Christof T1 - Finding dominant structures of nonreversible Markov processes JF - Multiscale Modeling and Simulation Y1 - 2016 U6 - https://doi.org/10.1137/15M1032272 VL - 14 IS - 4 SP - 1319 EP - 1340 ER - TY - CHAP A1 - Igde, Sinaida A1 - Wölk, Hendrik A1 - Röblitz, Susanna A1 - Reidelbach, Marco A1 - Weber, Marcus A1 - Hartmann, Laura T1 - Identifying Multivalent Binding Kinetics of Precision Glycomacromolecules: A Kinetic Study Using kinITC T2 - Münster Symposium on Cooperative Effects 2015 - SFB 858, at Westfälische Wilhelms-Universität Münster, 2015 N2 - Multivalent sugar/protein interactions are well-known to proceed through different binding modes 1-5 which in turn can be described by their binding kinetics 3-5. This study provides additional insight into the association and dissociation reaction rates of complex multivalent sugar/protein interactions. Binding kinetics of recently introduced multivalent precision glycomacromolecules 6-8 to Concanavalin A (Con A) were studied by " kinetic Isothermal Titration Calorimetry " (kinITC) 9-11. The effect of multivalency is evaluated by comparing rate constants of glycomacromolecules obtaining the same and different valency of mannose ligands and by variation of the overall backbone properties, such as hydrophilic/ hydrophoboc. In addition, binding kinetics were studied using different conformations of Con A (homodimer vs.-tetramer) and thus a different protein valency. Our results show that precision glycomacromolecule/Con A binding proceeds non-cooperatively. Further, association and dissociation rates are mainly described by intermolecular complex formation. Together with the so-called functional valency, we can discriminate between " bound " and " unbound " states for macroscopic on-and off-rates, even for such complex glycooligomer/protein systems. By comparing e.g. a mono-to a divalent glycomacromolecule for their binding to dimeric Con A, we see a lower dissociation rate for the latter. As both bind monovalently to Con A, this is a strong indication for a statistical rebinding event. Further, there is a strong dependence of multivalent binding kinetics on the ligand density of glycomacromolecules as well as the Con A conformation and thus the overall on-and off-rates. Y1 - 2015 ER - TY - JOUR A1 - Villatoro, José A1 - Zühlke, Martin A1 - Riebe, Daniel A1 - Beitz, Toralf A1 - Weber, Marcus A1 - Riedel, Jens A1 - Löhmannsröben, Hans-Gerd T1 - IR-MALDI ion mobility spectrometry: physical source characterization and application as HPLC detector JF - International Journal for Ion Mobility Spectrometry Y1 - 2016 U6 - https://doi.org/10.1007/s12127-016-0208-1 IS - 19/4 SP - 197 EP - 297 ER - TY - GEN A1 - Schütte, Christof A1 - Deuflhard, Peter A1 - Noé, Frank A1 - Weber, Marcus ED - Deuflhard, Peter ED - Grötschel, Martin ED - Hömberg, Dietmar ED - Horst, Ulrich ED - Kramer, Jürg ED - Mehrmann, Volker ED - Polthier, Konrad ED - Schmidt, Frank ED - Schütte, Christof ED - Skutella, Martin ED - Sprekels, Jürgen T1 - Design of functional molecules T2 - MATHEON-Mathematics for Key Technologies Y1 - 2014 VL - 1 SP - 49 EP - 65 PB - European Mathematical Society ER - TY - JOUR A1 - Igde, Sinaida A1 - Röblitz, Susanna A1 - Müller, Anne A1 - Kolbe, Katharina A1 - Boden, Sophia A1 - Fessele, Claudia A1 - Lindhorst, Thisbe A1 - Weber, Marcus A1 - Hartmann, Laura T1 - Linear Precision Glycomacromolecules with Varying Interligand Spacing and Linker Functionalities Binding to Concanavalin A and the Bacterial Lectin FimH JF - Marcomolecular Bioscience Y1 - 2017 U6 - https://doi.org/10.1002/mabi.201700198 VL - 17 IS - 12 SP - 1700198 ER - TY - JOUR A1 - Weber, Marcus T1 - Implications of PCCA+ in Molecular Simulation JF - Computation N2 - Upon ligand binding or during chemical reactions the state of a molecular system changes in time. Usually we consider a finite set of (macro-) states of the system (e.g., ’bound’ vs. ’unbound’), although the process itself takes place in a continuous space. In this context, the formula chi=XA connects the micro-dynamics of the molecular system to its macro-dynamics. Chi can be understood as a clustering of micro-states of a molecular system into a few macro-states. X is a basis of an invariant subspace of a transfer operator describing the micro-dynamics of the system. The formula claims that there is an unknown linear relation A between these two objects. With the aid of this formula we can understand rebinding effects, the electron flux in pericyclic reactions, and systematic changes of binding rates in kinetic ITC experiments. We can also analyze sequential spectroscopy experiments and rare event systems more easily. This article provides an explanation of the formula and an overview of some of its consequences. Y1 - 2018 U6 - https://doi.org/10.3390/computation6010020 VL - 6 IS - 1 SP - 20 ER - TY - GEN A1 - Weber, Marcus A1 - Durmaz, Vedat A1 - Sabri, Peggy A1 - Reidelbach, Marco T1 - Supplementary simulation data for Science Manuscript ai8636 N2 - The simulation data has been produced by Vedat Durmaz, Peggy Sabri and Marco Reidelbach inside the "Computational Molecular Design" Group headed by Marcus Weber at Zuse-Institut Berlin, Takustr. 7, D-14195 Berlin, Germany. The file contains classical simulation data for different fentanyl derivates in the MOR binding pocket at different pHs. It also includes instruction files for quantum-chemical pKa-value estimations and a description of how we derived the pKa-values from the Gaussian09 log-files. Y1 - 2017 U6 - https://doi.org/10.12752/5.MWB.1.0 N1 - GROMACS trajectories and GAUSSIAN files of MOR and fentanyl derivates ER - TY - JOUR A1 - Schrade, Katharina A1 - Tröger, Jessica A1 - Eldashan, Adeep A1 - Zühlke, Kerstin A1 - Abdul Azees, Kamal R. A1 - Elkins, Jonathan M. A1 - Neuenschwander, Martin A1 - Oder, Andreas A1 - Elkewedi, Mohamed A1 - Jaksch, Sarah A1 - Andrae, Karsten A1 - Li, Jinliang A1 - Fernandes, Jaoa A1 - Müller, Paul Markus A1 - Grunwald, Stephan A1 - Marino, Stephen F. A1 - Vukicevic, Tanja A1 - Eichhorst, Jenny A1 - Wiesner, Burkhard A1 - Weber, Marcus A1 - Kapiloff, Michael A1 - Rocks, Oliver A1 - Daumke, Oliver A1 - Wieland, Thomas A1 - Knapp, Stefan A1 - von Kries, Jens Peter A1 - Klussmann, Enno T1 - An AKAP-Lbc-RhoA interaction inhibitor promotes the translocation of aquaporin-2 to the plasma membrane of renal collecting duct principal cells JF - PLOS ONE N2 - Stimulation of renal collecting duct principal cells with antidiuretic hormone (arginine-vasopressin, AVP) results in inhibition of the small GTPase RhoA and the enrichment of the water channel aquaporin-2 (AQP2) in the plasma membrane. The membrane insertion facilitates water reabsorption from primary urine and fine-tuning of body water homeostasis. Rho guanine nucleotide exchange factors (GEFs) interact with RhoA, catalyze the exchange of GDP for GTP and thereby activate the GTPase. However, GEFs involved in the control of AQP2 in renal principal cells are unknown. The A-kinase anchoring protein, AKAP-Lbc, possesses GEF activity, specifically activates RhoA, and is expressed in primary renal inner medullary collecting duct principal (IMCD) cells. Through screening of 18,431 small molecules and synthesis of a focused library around one of the hits, we identified an inhibitor of the interaction of AKAP-Lbc and RhoA. This molecule, Scaff10-8, bound to RhoA, inhibited the AKAP-Lbc-mediated RhoA activation but did not interfere with RhoA activation through other GEFs or activities of other members of the Rho family of small GTPases, Rac1 and Cdc42. Scaff10-8 promoted the redistribution of AQP2 from intracellular vesicles to the periphery of IMCD cells. Thus, our data demonstrate an involvement of AKAP-Lbc-mediated RhoA activation in the control of AQP2 trafficking. Y1 - 2018 U6 - https://doi.org/10.1371/journal.pone.0191423 VL - 13 IS - 1 SP - e0191423 EP - e0191423 ER - TY - GEN A1 - Weber, Marcus T1 - Supplementary: Implications of PCCA+ in Molecular Simulation N2 - Matlab-software and data sets to recapitulate the presented results in M. Weber: Implications of PCCA+ in Molecular Simulation. Computation, 6(1):20, 2018. Y1 - 2018 N1 - This data set includes one folder per published figure. The folders contain all needed resources to recapitulate the presented results. ER - TY - JOUR A1 - Spahn, Viola A1 - Del Vecchio, Giovanna A1 - Labuz, Dominika A1 - Rodriguez-Gaztelumendi, Antonio A1 - Massaly, N. A1 - Temp, Julia A1 - Durmaz, Vedat A1 - Sabri, P. A1 - Reidelbach, Marco A1 - Machelska, Halina A1 - Weber, Marcus A1 - Stein, Christoph T1 - A nontoxic pain killer designed by modeling of pathological receptor conformations JF - Science Y1 - 2017 U6 - https://doi.org/10.1126/science.aai8636 VL - 355 IS - 6328 SP - 966 EP - 969 ER - TY - GEN A1 - Weber, Marcus T1 - Eigenvalues of non-reversible Markov chains – A case study N2 - Finite reversible Markov chains are characterized by a transition matrix P that has real eigenvalues and pi-orthogonal eigenvectors, where pi is the stationary distribution of P. This means, that a transition matrix with complex eigenvalues corresponds to a non-reversible Markov chain. This observation leads to the question, whether the imaginary part of that eigendecomposition corresponds to or indicates the “pattern” of the nonreversibility. This article shows that the direct relation between imaginary parts of eigendecompositions and the non-reversibility of a transition matrix is not given. It is proposed to apply the Schur decomposition of P instead of the eigendecomposition in order to characterize its nonreversibility. T3 - ZIB-Report - 17-13 KW - non-reversible KW - transition matrix KW - detailed balance Y1 - 2017 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:0297-zib-62191 SN - 1438-0064 ER - TY - JOUR A1 - Siegel, D. A1 - Andrae, Karsten A1 - Proske, Matthias A1 - Kochan, C. A1 - Koch, Matthias A1 - Weber, Marcus A1 - Nehls, Irene T1 - Dynamic covalent hydrazine chemistry as a specific extraction and cleanup technique for the quantification of the Fusarium mycotoxin zearalenone in edible oils JF - Journal of Chromatography A Y1 - 2010 VL - 1217(15) SP - 2206 EP - 15 ER - TY - JOUR A1 - Scheibe, Ch. A1 - Bujotzek, Alexander A1 - Dernedde, Jens A1 - Weber, Marcus A1 - Seitz, O. T1 - DNA-programmed spatial screening of carbohydrate-lectin interactions JF - Chem. Sci. Y1 - 2011 VL - 2 SP - 770 EP - 775 ER - TY - CHAP A1 - Weber, Marcus A1 - Rungsarityotin, Wasinee A1 - Schliep, Alexander ED - Spiliopoulou, Myra ED - Kruse, Rudolf ED - Borgelt, Christian ED - Nürnberger, Andreas ED - Gaul, Wolfgang T1 - An Indicator for the Number of Clusters T2 - From Data and Information Analysis to Knowledge Engineering Y1 - 2006 UR - http://dx.doi.org/10.1007/3-540-31314-1_11 SP - 103 EP - 110 PB - Springer Berlin Heidelberg ER - TY - JOUR A1 - Weber, Marcus A1 - Andrae, Karsten T1 - A simple method for the estimation of entropy differences JF - MATCH Commun. Math. Comp. Chem. 2010 Y1 - 2010 VL - 63(2) SP - 319 EP - 332 ER - TY - JOUR A1 - Weber, Marcus A1 - Becker, Roland A1 - Köppen, Robert A1 - Durmaz, Vedat T1 - Classical hybrid Monte-Carlo simulations of the interconversion of hexabromocyclododecane JF - Journal of Molecular Simulation Y1 - 2008 VL - 34 IS - 7 SP - 727 EP - 736 ER - TY - JOUR A1 - Weber, Marcus A1 - Bujotzek, Alexander A1 - Andrae, Karsten A1 - Weinhart, M. A1 - Haag, Rainer T1 - Computational entropy estimation of linear polyether modified surfaces and correlation with protein resistant properties of such surfaces JF - J. Mol. Sim. Y1 - 2011 ER - TY - JOUR A1 - Förster, C. A1 - Brauer, Arnd B. E. A1 - Fürste, J. A1 - Betzel, C. A1 - Weber, Marcus A1 - Cordes, Frank A1 - Erdmann, V. T1 - Visualization of the tRNA(Ser) acceptor step binding site in the seryl-tRNA synthetase JF - BBRC Y1 - 2007 VL - 362 IS - 2 SP - 415 EP - 418 ER - TY - CHAP A1 - Kube, Susanna A1 - Weber, Marcus T1 - Preserving the Markov Property of Reduced Reversible Markov Chains T2 - Numerical Analysis and Applied Mathematics, International Conference on Numerical Analysis and Applied Mathematics 2008 Y1 - 2008 VL - 1048 SP - 593 EP - 596 ER - TY - THES A1 - Weber, Marcus T1 - Meshless Methods in Conformation Dynamics Y1 - 2006 ER - TY - JOUR A1 - Weber, Marcus A1 - Kube, Susanna A1 - Walter, Lionel A1 - Deuflhard, Peter T1 - Stable Computation of Probability Densities of Metastable Dynamical Systems JF - SIAM J. Multiscale Model. Simul. Y1 - 2007 VL - 6 IS - 2 SP - 396 EP - 416 ER - TY - GEN A1 - Bojarovski, Stefan A1 - Hege, Hans-Christian A1 - Lie, Han Cheng A1 - Weber, Marcus T1 - Topological analysis and visualization of scalar functions characterizing conformational transitions of molecules on multiple time-scales T2 - Shape Up 2015 - Exercises in Materials Geometry and Topology, 14-18 Sept. 2015, Berlin, Germany N2 - Molecular processes such as protein folding or ligand-receptor-binding can be understood by analyzing the free energy landscape. Those processes are often metastable, i.e. the molecular systems remain in basins around local minima of the free energy landscape, and in rare cases undergo gauche transitions between metastable states by passing saddle-points of this landscape. By discretizing the configuration space, this can be modeled as a discrete Markov process. One way to compute the transition rates between conformations of a molecular system is by utilizing Transition Path Theory and the concept of committor functions. A fundamental problem from the computational point of view is that many time-scales are involved, ranging from 10^(-14) sec for the fastest motion to 10^(-6) sec or more for conformation changes that cause biological effects. The goal of our work is to provide a better understanding of such transitions in configuration space on various time-scales by analyzing characteristic scalar functions topologically and geometrically. We are developing suitable visualization and interaction techniques to support our analysis. For example, we are analyzing a transition rate indicator function by computing and visualizing its Reeb graph together with the sets of molecular states corresponding to maxima of the transition rate indicator function. A particular challenge is the high dimensionality of the domain which does not allow for a straightforward visualization of the function. The computational topology approach to the analysis of the transition rate indicator functions for a molecular system allows to explore different time scales of the system by utilizing coarser or finer topological partitioning of the function. A specific goal is the development of tools for analyzing the hierarchy of these partitionings. This approach tackles the analysis of a complex and sparse dataset from a different angle than the well-known spectral analysis of Markov State Models. Y1 - 2015 ER - TY - JOUR A1 - Krebek, von, Larissa K. S. A1 - Achazi, Andreas J. A1 - Solleder, Marthe A1 - Weber, Marcus A1 - Paulus, Beate A1 - Schalley, Christoph A. T1 - Allosteric and Chelate Cooperativity in Divalent Crown Ether–Ammonium Complexes with Strong Binding Enhancements JF - Chem. Eur. J. Y1 - 2016 U6 - https://doi.org/10.1002/chem.201603098 N1 - Has been announced under the title: Cooperativity in Multivalent Binding: A Detailed Experimental and Theoretical Thermochemical Study of Divalent Crown Ether-Ammonium Complexes VL - 22 IS - 43 SP - 15475 EP - 15484 ER - TY - GEN A1 - Djurdjevac Conrad, Natasa A1 - Weber, Marcus A1 - Schütte, Christof T1 - Finding dominant structures of nonreversible Markov processes N2 - Finding metastable sets as dominant structures of Markov processes has been shown to be especially useful in modeling interesting slow dynamics of various real world complex processes. Furthermore, coarse graining of such processes based on their dominant structures leads to better understanding and dimension reduction of observed systems. However, in many cases, e.g. for nonreversible Markov processes, dominant structures are often not formed by metastable sets but by important cycles or mixture of both. This paper aims at understanding and identifying these different types of dominant structures for reversible as well as nonreversible ergodic Markov processes. Our algorithmic approach generalizes spectral based methods for reversible process by using Schur decomposition techniques which can tackle also nonreversible cases. We illustrate the mathematical construction of our new approach by numerical experiments. T3 - ZIB-Report - 15-40 KW - nonreversible Markov processes KW - metastable sets KW - cycle decomposition KW - Schur decomposition Y1 - 2015 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:0297-zib-55739 SN - 1438-0064 ER - TY - JOUR A1 - Abendroth, Frank A1 - Solleder, Marthe A1 - Welker, Pia A1 - Licha, Kai A1 - Weber, Marcus A1 - Seitz, Oliver A1 - Mangoldt, Dorothea T1 - High affinity flourescence labelled ligands for the estrogen receptor JF - Eur. J. Org. Chem. Y1 - 2015 VL - 2015 IS - 10 SP - 2157 EP - 2166 ER - TY - JOUR A1 - Koschek, A1 - Durmaz, Vedat A1 - Krylova, A1 - Wieczorek, A1 - Gupta, Pooja A1 - Richter, A1 - Bujotzek, Alexander A1 - Fischer, A1 - Haag, Rainer A1 - Freund, A1 - Weber, Marcus A1 - Rademann, T1 - Peptide polymer ligands for a tandem WW-domain, a soft multivalent protein-protein interaction: lessons on the thermodynamic fitness of flexible ligands JF - Beilstein J. Org. Chem. Y1 - 2015 VL - 11 SP - 837 EP - 847 ER - TY - JOUR A1 - Durmaz, Vedat A1 - Weber, Marcus A1 - Meyer, A1 - Mückter, T1 - Computergestützte Simulationen zur Abschätzung gesundheitlicher Risiken durch anthropogene Spurenstoffe der Wassermatrix JF - KA Korrespondenz Abwasser, Abfall Y1 - 2015 VL - 3/15 SP - 264 EP - 267 ER - TY - JOUR A1 - Röblitz, Susanna A1 - Weber, Marcus T1 - Fuzzy spectral clustering by PCCA+: application to Markov state models and data classification JF - Advances in Data Analysis and Classification Y1 - 2013 U6 - https://doi.org/10.1007/s11634-013-0134-6 VL - 7 IS - 2 SP - 147 EP - 179 ER - TY - GEN A1 - Nielsen, Adam A1 - Weber, Marcus T1 - Computing the nearest reversible Markov chain N2 - Reversible Markov chains are the basis of many applications. However, computing transition probabilities by a finite sampling of a Markov chain can lead to truncation errors. Even if the original Markov chain is reversible, the approximated Markov chain might be non-reversible and will lose important properties, like the real valued spectrum. In this paper, we show how to find the closest reversible Markov chain to a given transition matrix. It turns out that this matrix can be computed by solving a convex minimization problem. T3 - ZIB-Report - 14-48 KW - Reversible Markov Chain KW - Convex Optimization KW - MSM Y1 - 2014 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:0297-zib-53292 SN - 1438-0064 ER - TY - JOUR A1 - Nielsen, Adam A1 - Weber, Marcus T1 - Computing the nearest reversible Markov chain JF - Numerical Linear Algebra with Applications N2 - Reversible Markov chains are the basis of many applications. However, computing transition probabilities by a finite sampling of a Markov chain can lead to truncation errors. Even if the original Markov chain is reversible, the approximated Markov chain might be non-reversible and will lose important properties, like the real valued spectrum. In this paper, we show how to find the closest reversible Markov chain to a given transition matrix. It turns out that this matrix can be computed by solving a convex minimization problem. KW - Reversible Markov Chain KW - Convex Optimization KW - MSM Y1 - 2015 U6 - https://doi.org/10.1002/nla.1967 VL - 22 IS - 3 SP - 483 EP - 499 ER - TY - GEN A1 - Deuflhard, Peter A1 - Weber, Marcus ED - Deuflhard, Peter ED - Grötschel, Martin ED - Hömberg, Dietmar ED - Horst, Ulrich ED - Kramer, Jürg ED - Mehrmann, Volker ED - Polthier, Konrad ED - Schmidt, Frank ED - Skutella, Martin ED - Sprekels, Jürgen T1 - Mathematics without pain T2 - MATHEON-Mathematics for Key Technologies Y1 - 2014 U6 - https://doi.org/10.4171/137 VL - 1 SP - 26 EP - 28 PB - European Mathematical Society ER - TY - JOUR A1 - Röblitz, Susanna A1 - Weber, Marcus T1 - Fuzzy Spectral Clustering by PCCA+ JF - Classification and Clustering: Models, Software and Applications Y1 - 2009 UR - http://www.wias-berlin.de/publications/wias-publ/run.jsp?template=abstract&type=Report&year=2009&number=26 IS - WIAS Report No. 26 SP - 73 EP - 79 ER - TY - JOUR A1 - Erlekam, Franziska A1 - Igde, Sinaida A1 - Röblitz, Susanna A1 - Hartmann, Laura A1 - Weber, Marcus T1 - Modeling of Multivalent Ligand-Receptor Binding Measured by kinITC JF - Computation N2 - In addition to the conventional Isothermal Titration Calorimetry (ITC), kinetic ITC (kinITC) not only gains thermodynamic information, but also kinetic data from a biochemical binding process. Moreover, kinITC gives insights into reactions consisting of two separate kinetic steps, such as protein folding or sequential binding processes. The ITC method alone cannot deliver kinetic parameters, especially not for multivalent bindings. This paper describes how to solve the problem using kinITC and an invariant subspace projection. The algorithm is tested for multivalent systems with different valencies. Y1 - 2019 U6 - https://doi.org/10.3390/computation7030046 VL - 7 IS - 3 SP - 46 ER - TY - JOUR A1 - Weber, Marcus T1 - Transformationsprodukte im Klärwerk: Mathematische Ansätze der Bewertung JF - KA Korrespondenz Abwasser, Abfall Y1 - 2019 VL - 7 SP - 551 EP - 557 ER - TY - JOUR A1 - Venkatareddy, Narendra Lagumaddepalli A1 - Wilke, Patrick A1 - Ernst, Natalia A1 - Horch, Justus A1 - Weber, Marcus A1 - Dallmann, Andre A1 - Börner, Hans G. T1 - Mussel-glue inspired adhesives: A study on the relevance of L-Dopa and the function of the sequence at nanomaterial-peptide interfaces JF - Advanced Materials Interfaces N2 - Mussel glue‐proteins undergo structural transitions at material interfaces to optimize adhesive surface contacts. Those intriguing structure responses are mimicked by a mussel‐glue mimetic peptide (HSY*SGWSPY*RSG (Y* = l‐Dopa)) that was previously selected by phage‐display to adhere to Al2O3 after enzymatic activation. Molecular level insights into the full‐length adhesion domain at Al2O3 surfaces are provided by a divergent‐convergent analysis, combining nuclear Overhauser enhancement based 2D NOESY and saturation transfer difference NMR analysis of submotifs along with molecular dynamics simulations of the full‐length peptide. The peptide is divided into two submotifs, each containing one Dopa “anchor” (Motif‐1 and 2). The analysis proves Motif‐1 to constitute a dynamic Al2O3 binder and adopting an “M”‐structure with multiple surface contacts. Motif‐2 binds stronger by two surface contacts, forming a compact “C”‐structure. Taking these datasets as constraints enables to predict the structure and propose a binding process model of the full‐length peptide adhering to Al2O3. Y1 - 2019 U6 - https://doi.org/10.1002/admi.201900501 VL - 6 IS - 13 SP - 1900501 ER - TY - JOUR A1 - Del Vecchio, Giovanna A1 - Labuz, Dominika A1 - Temp, Julia A1 - Seitz, Viola A1 - Kloner, Michael A1 - Negrete, Roger A1 - Rodriguez-Gaztelumendi, Antonio A1 - Weber, Marcus A1 - Machelska, Halina A1 - Stein, Christoph T1 - pKa of opioid ligands as a discriminating factor for side effects JF - Scientific Reports N2 - The non-selective activation of central and peripheral opioid receptors is a major shortcoming of currently available opioids. Targeting peripheral opioid receptors is a promising strategy to preclude side effects. Recently, we showed that fentanyl-derived μ-opioid receptor (MOR) agonists with reduced acid dissociation constants (pKa) due to introducing single fluorine atoms produced injury-restricted antinociception in rat models of inflammatory, postoperative and neuropathic pain. Here, we report that a new double-fluorinated compound (FF6) and fentanyl show similar pKa, MOR affinity and [35S]-GTPγS binding at low and physiological pH values. In vivo, FF6 produced antinociception in injured and non-injured tissue, and induced sedation and constipation. The comparison of several fentanyl derivatives revealed a correlation between pKa values and pH-dependent MOR activation, antinociception and side effects. An opioid ligand's pKa value may be used as discriminating factor to design safer analgesics. Y1 - 2019 U6 - https://doi.org/10.1038/s41598-019-55886-1 VL - 9 SP - 19344 ER - TY - JOUR A1 - Villatoro, José A1 - Zühlke, Martin A1 - Riebe, Daniel A1 - Beitz, Toralf A1 - Weber, Marcus A1 - Löhmannsröben, Hans-Gerd T1 - Sub-ambient pressure IR-MALDI ion mobility spectrometer for the determination of low and high field mobilities JF - Analytical and Bioanalytical Chemistry N2 - A new ion mobility (IM) spectrometer, enabling mobility measurements in the pressure range between 5 and 500 mbar and in the reduced field strength range E/N of 5–90 Td, was developed and characterized. Reduced mobility (K0) values were studied under low E/N (constant value) as well as high E/N (deviation from low field K0) for a series of molecular ions in nitrogen. Infrared matrix-assisted laser desorption ionization (IR-MALDI) was used in two configurations: a source working at atmospheric pressure (AP) and, for the first time, an IR-MALDI source working with a liquid (aqueous) matrix at sub-ambient/reduced pressure (RP). The influence of RP on IR-MALDI was examined and new insights into the dispersion process were gained. This enabled the optimization of the IM spectrometer for best analytical performance. While ion desolvation is less efficient at RP, the transport of ions is more efficient, leading to intensity enhancement and an increased number of oligomer ions. When deciding between AP and RP IR-MALDI, a trade-off between intensity and resolving power has to be considered. Here, the low field mobility of peptide ions was first measured and compared with reference values from ESI-IM spectrometry (at AP) as well as collision cross sections obtained from molecular dynamics simulations. The second application was the determination of the reduced mobility of various substituted ammonium ions as a function of E/N in nitrogen. The mobility is constant up to a threshold at high E/N. Beyond this threshold, mobility increases were observed. This behavior can be explained by the loss of hydrated water molecules. Y1 - 2020 U6 - https://doi.org/10.1007/s00216-020-02735-0 VL - 412 SP - 5247 EP - 5260 ER - TY - JOUR A1 - Sikorski, Alexander A1 - Weber, Marcus A1 - Schütte, Christof T1 - The Augmented Jump Chain JF - Advanced Theory and Simulations N2 - Modern methods of simulating molecular systems are based on the mathematical theory of Markov operators with a focus on autonomous equilibrated systems. However, non-autonomous physical systems or non-autonomous simulation processes are becoming more and more important. A representation of non-autonomous Markov jump processes is presented as autonomous Markov chains on space-time. Augmenting the spatial information of the embedded Markov chain by the temporal information of the associated jump times, the so-called augmented jump chain is derived. The augmented jump chain inherits the sparseness of the infinitesimal generator of the original process and therefore provides a useful tool for studying time-dependent dynamics even in high dimensions. Furthermore, possible generalizations and applications to the computation of committor functions and coherent sets in the non-autonomous setting are discussed. After deriving the theoretical foundations, the concepts with a proof-of-concept Galerkin discretization of the transfer operator of the augmented jump chain applied to simple examples are illustrated. Y1 - 2021 U6 - https://doi.org/10.1002/adts.202000274 VL - 4 IS - 4 PB - Wiley-VCH ER - TY - JOUR A1 - Reidelbach, Marco A1 - Weber, Marcus A1 - Imhof, Petra T1 - Prediction of perturbed proton transfer networks JF - PLoS ONE N2 - The transfer of protons through proton translocating channels is a complex process, for which direct samplings of different protonation states and side chain conformations in a transition network calculation provide an efficient, bias-free description. In principle, a new transition network calculation is required for every unsampled change in the system of interest, e.g. an unsampled protonation state change, which is associated with significant computational costs. Transition networks void of or including an unsampled change are termed unperturbed or perturbed, respectively. Here, we present a prediction method, which is based on an extensive coarse-graining of the underlying transition networks to speed up the calculations. It uses the minimum spanning tree and a corresponding sensitivity analysis of an unperturbed transition network as initial guess and refinement parameter for the determination of an unknown, perturbed transition network. Thereby, the minimum spanning tree defines a sub-network connecting all nodes without cycles and minimal edge weight sum, while the sensitivity analysis analyzes the stability of the minimum spanning tree towards individual edge weight reductions. Using the prediction method, we are able to reduce the calculation costs in a model system by up to 80%, while important network properties are maintained in most predictions. Y1 - 2018 U6 - https://doi.org/https://doi.org/10.1371/journal.pone.0207718 VL - 13 IS - 12 SP - e0207718 EP - e0207718 ER - TY - JOUR A1 - Villatoro, José A1 - Weber, Marcus A1 - Zühlke, Martin A1 - Lehmann, Andreas A1 - Zechiowski, Karl A1 - Riebe, Daniel A1 - Beitz, Toralf A1 - Löhmannsröben, Hans-Gerd A1 - Kreuzer, Oliver T1 - Structural characterization of synthetic peptides using electronspray ion mobility spectrometry and molecular dynamics simulations JF - International Journal of Mass Spectrometry N2 - Electrospray ionization-ion mobility spectrometry was employed for the determination of collision cross sections (CCS) of 25 synthetically produced peptides in the mass range between 540–3310 Da. The experimental measurement of the CCS is complemented by their calculation applying two different methods. One prediction method is the intrinsic size parameter (ISP) method developed by the Clemmer group. The second new method is based on the evaluation of molecular dynamics (MD) simulation trajectories as a whole, resulting in a single, averaged collision cross-section value for a given peptide in the gas phase. A high temperature MD simulation is run in order to scan through the whole conformational space. The lower temperature conformational distribution is obtained through thermodynamic reweighting. In the first part, various correlations, e.g. CCS vs. mass and inverse mobility vs. m/z correlations, are presented. Differences in CCS between peptides are also discussed in terms of their respective mass and m/z differences, as well as their respective structures. In the second part, measured and calculated CCS are compared. The agreement between the prediction results and the experimental values is in the same range for both calculation methods. While the calculation effort of the ISP method is much lower, the MD method comprises several tools providing deeper insights into the conformations of peptides. Advantages and limitations of both methods are discussed. Based on the separation of two pairs of linear and cyclic peptides of virtually the same mass, the influence of the structure on the cross sections is discussed. The shift in cross section differences and peak shape after transition from the linear to the cyclic peptide can be well understood by applying different MD tools, e.g. the root-mean-square deviation (RMSD) and the root mean square fluctuation (RMSF). Y1 - 2019 U6 - https://doi.org/10.1016/j.ijms.2018.10.036 VL - 436 SP - 108 EP - 117 ER - TY - JOUR A1 - Abbas, Aennes A1 - Schneider, Ilona A1 - Bollmann, Anna A1 - Funke, Jan A1 - Oehlmann, Jörg A1 - Prasse, Carsten A1 - Schulte-Oehlmann, Ulrike A1 - Seitz, Wolfram A1 - Ternes, Thomas A1 - Weber, Marcus A1 - Wesely, Henning A1 - Wagner, Martin T1 - What you extract is what you see: Optimising the preparation of water and wastewater samples for in vitro bioassays JF - Water Research N2 - The assessment of water quality is crucial for safeguarding drinking water resources and ecosystem integrity. To this end, sample preparation and extraction is critically important, especially when investigating emerging contaminants and the toxicity of water samples. As extraction methods are rarely optimised for bioassays but rather adopted from chemical analysis, this may result in a misrepresentation of the actual toxicity. In this study, surface water, groundwater, hospital and municipal wastewater were used to characterise the impacts of common sample preparation techniques (acidification, filtration and solid phase extraction (SPE)) on the outcomes of eleven in vitro bioassays. The latter covered endocrine activity (reporter gene assays for estrogen, androgen, aryl-hydrocarbon, retinoic acid, retinoid X, vitamin D, thyroid receptor), mutagenicity (Ames fluctuation test), genotoxicity (umu test) and cytotoxicity. Water samples extracted using different SPE sorbents (Oasis HLB, Supelco ENVI-Carb+, Telos C18/ENV) at acidic and neutral pH were compared for their performance in recovering biological effects. Acidification, commonly used for stabilisation, significantly altered the endocrine activity and toxicity of most (waste)water samples. Sample filtration did not affect the majority of endpoints but in certain cases affected the (anti-)estrogenic and dioxin-like activities. SPE extracts (10.4 × final concentration), including WWTP effluents, induced significant endocrine effects that were not detected in aqueous samples (0.63 × final concentration), such as estrogenic, (anti-)androgenic and dioxin-like activities. When ranking the SPE methods using multivariate Pareto optimisation an extraction with Telos C18/ENV at pH 7 was most effective in recovering toxicity. At the same time, these extracts were highly cytotoxic masking the endpoint under investigation. Compared to that, extraction at pH 2.5 enriched less cytotoxicity. In summary, our study demonstrates that sample preparation and extraction critically affect the outcome of bioassays when assessing the toxicity of water samples. Depending on the water matrix and the bioassay, these methods need to be optimised to accurately assess water quality. Y1 - 2019 U6 - https://doi.org/10.1016/j.watres.2018.12.049 VL - 152 SP - 47 EP - 60 ER - TY - JOUR A1 - Wagner, Sabine A1 - Zapata, Carlos A1 - Wan, Wei A1 - Gawlitza, Kornelia A1 - Weber, Marcus A1 - Rurack, Knut T1 - Role of Counterions in Molecularly Imprinted Polymers for Anionic Species JF - Langmuir N2 - Small-molecule oxoanions are often imprinted noncovalently as carboxylates into molecularly imprinted polymers (MIPs), requiring the use of an organic counterion. Popular species are either pentamethylpiperidine (PMP) as a protonatable cation or tetraalkylammonium (TXA) ions as permanent cations. The present work explores the influence of the TXA as a function of their alkyl chain length, from methyl to octyl, using UV/vis absorption, fluorescence titrations, and HPLC as well as MD simulations. Protected phenylalanines (Z-L/D-Phe) served as templates/analytes. While the influence of the counterion on the complex stability constants and anion-induced spectral changes shows a monotonous trend with increasing alkyl chain length at the prepolymerization stage, the cross-imprinting/rebinding studies showed a unique pattern that suggested the presence of adaptive cavities in the MIP matrix, related to the concept of induced fit of enzyme–substrate interaction. Larger cavities formed in the presence of larger counterions can take up pairs of Z-x-Phe and smaller TXA, eventually escaping spectroscopic detection. Correlation of the experimental data with the MD simulations revealed that counterion mobility, the relative distances between the three partners, and the hydrogen bond lifetimes are more decisive for the response features observed than actual distances between interacting atoms in a complex or the orientation of binding moieties. TBA has been found to yield the highest imprinting factor, also showing a unique dual behavior regarding the interaction with template and fluorescent monomer. Finally, interesting differences between both enantiomers have been observed in both theory and experiment, suggesting true control of enantioselectivity. The contribution concludes with suggestions for translating the findings into actual MIP development. Y1 - 2018 U6 - https://doi.org/10.1021/acs.langmuir.8b00500 VL - 34 IS - 23 SP - 6963 EP - 6975 ER - TY - JOUR A1 - Spahn, Viola A1 - Del Vecchio, Giovanna A1 - Rodriguez-Gaztelumendi, Antonio A1 - Temp, Julia A1 - Labuz, Dominika A1 - Kloner, Michael A1 - Reidelbach, Marco A1 - Machelska, Halina A1 - Weber, Marcus A1 - Stein, Christoph T1 - Opioid receptor signaling, analgesic and side effects induced by a computationally designed pH-dependent agonist JF - Scientific Reports N2 - Novel pain killers without adverse effects are urgently needed. Y1 - 2018 VL - 8 SP - 8965 PB - Springer Nature ER - TY - JOUR A1 - Weber, Marcus T1 - Transformationsprodukte im Klärwerk: Mathematische Ansätze der Bewertung JF - KA Korrespondenz Abwasser, Abfall Y1 - 2018 ER - TY - JOUR A1 - Sechi, Renata A1 - Fackeldey, Konstantin A1 - Chewle, Surahit A1 - Weber, Marcus T1 - SepFree NMF: A Toolbox for Analyzing the Kinetics of Sequential Spectroscopic Data JF - Algorithms N2 - This work addresses the problem of determining the number of components from sequential spectroscopic data analyzed by non-negative matrix factorization without separability assumption (SepFree NMF). These data are stored in a matrix M of dimension “measured times” versus “measured wavenumbers” and can be decomposed to obtain the spectral fingerprints of the states and their evolution over time. SepFree NMF assumes a memoryless (Markovian) process to underline the dynamics and decomposes M so that M=WH, with W representing the components’ fingerprints and H their kinetics. However, the rank of this decomposition (i.e., the number of physical states in the process) has to be guessed from pre-existing knowledge on the observed process. We propose a measure for determining the number of components with the computation of the minimal memory effect resulting from the decomposition; by quantifying how much the obtained factorization is deviating from the Markovian property, we are able to score factorizations of a different number of components. In this way, we estimate the number of different entities which contribute to the observed system, and we can extract kinetic information without knowing the characteristic spectra of the single components. This manuscript provides the mathematical background as well as an analysis of computer generated and experimental sequentially measured Raman spectra. Y1 - 2022 U6 - https://doi.org/10.3390/a15090297 VL - 15 IS - 9 SP - 297 ER -