TY - JOUR A1 - Choi, Ching-Yi A1 - Lossada, F. A1 - Walter, K. A1 - Fleck-Kunde, T. A1 - Behrens, S. A1 - Meinelt, T. A1 - Falkenhagen, Jana A1 - Hiller, M. A1 - Oschkinat, H. A1 - Dallmann, A. A1 - Taden, A. A1 - Börner, H.G. T1 - Organic transformation of lignin into mussel-inspired glues: next-generation 2K adhesive for setting corals under saltwater N2 - The 2-methoxyphenol units (G-units) in lignin are modified by demethylation and oxidation to provide the activated lignin as one part of an advanced biobased two-component (2K) adhesive system, which exhibits promising shear strengths in dry and underwater applications. The activation of lignin is straightforward and generates quinones via demethylation and periodate oxidation. These act as Michael acceptors and react smoothly with multi-thiol-star polymers to yield thiol-catechol connectivities (TCCs). The mussel-inspired material platform acts as a very robust and versatile adhesive, combining low-cost and readily available lignin with multi-thiols to achieve outstanding adhesion strengths of up to 15 MPa in dry application. In particular, the 2K system is compatible with the marine biological environment and shows no acute toxicity to sensitive organisms such as fish eggs. Thus, one possible application of this material could be an adhesive for setting temperature-resistant corals in damaged reefs. KW - Lignin modification KW - Mussel-inspired adhesive systems PY - 2023 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-594588 DO - https://doi.org/10.1039/d3gc03680d SN - 1463-9270 SP - 1 EP - 15 PB - RSC CY - Cambridge AN - OPUS4-59458 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Witte, Julien A1 - Schröpfer, Dirk A1 - Hamacher, M. A1 - Michels, H. A1 - Hamm, C. A1 - Appelt, M. A1 - Börner, Andreas A1 - Kannengießer, Thomas T1 - Tool development for hybrid finishing milling of iron aluminides N2 - The importance of high-temperature materials made of iron aluminides (FeAl) has been increasing in light weight applications, e.g., airplane turbines, due to the high material’s specific strength. However, the highly economic production by means of permanent mold casting involves special microstructures for Fe26Al4Mo0.5Ti1B alloy components leading to difficult machinability for subsequent finishing milling and low surface qualities. Major effects of tool and machining parameter variation incorporating ultrasonic assistance on the milling process and surface integrity are shown. Loads for tool and component surface are significantly adjustable to enable an economic process chain regarding the surface integrity of safety-relevant components. KW - Ultrasonic-assisted milling KW - Iron aluminide KW - Surface integrity KW - Tool wear PY - 2022 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-566294 DO - https://doi.org/10.1016/j.procir.2022.03.123 SN - 2212-8271 VL - 108 SP - 793 EP - 798 PB - Elsevier B.V. AN - OPUS4-56629 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Witte, Julien A1 - Schröpfer, Dirk A1 - Börner, Andreas A1 - Kannengießer, Thomas A1 - Michels, H. A1 - Hamm, C. A1 - Appelt, M. A1 - Hamacher, M. T1 - Ultraschallunterstütztes Fräsen zur Reduzierung der Belastung auf Werkzeug und Bauteiloberfläche von Eisenaluminid-Bauteilen N2 - Intermetallische Werkstoffe werden für Hochtemperaturanwendungen immer wichtiger. Insbesondere Aluminide mit hohen spezifischen Festigkeiten haben ein großes Potenzial für Leichtbauanwendungen, z. B. werden Titanaluminide bereits in Flugzeugturbinen eingesetzt. Ökonomische und ökologische Aspekte sind die treibende Kraft zur Substitution konventioneller Legierungen, z. B. Nickelbasislegierungen, die eine wesentlich höhere Kostenintensität und ein höheres Gewichts-Festigkeits-Verhältnis aufweisen. Insbesondere Eisenaluminide (FeAl) sind aufgrund guter mechanischer Eigenschaften und der guten Verfügbarkeit der wichtigsten Hauptlegierungselemente attraktiv. Speziell entwickelte FeAl-Legierungskonzepte ermöglichen eine wirtschaftliche Produktion im Kokillenguss, bei der die Erstarrung der Schmelze spezielle komplexe Gefüge ermöglicht, um die hohen thermischen und mechanischen Eigenschaften durch eine hohe Anzahl von harten Ausscheidungen entlang der Korngrenzen zu erreichen. Zu diesen Eigenschaften gehört aber auch, dass notwendige Bearbeitungsschritte, wie das Schlichtfräsen, zur Erzielung komplexer Endkonturen, zu vorzeitigem Werkzeugverschleiß und geringen Oberflächengüten führen. Für das finale FeAl-Bauteil ist eine hohe Oberflächenintegrität insbesondere in sicherheitsrelevanten Anwendungen in der Luftfahrt oder im Energiebereich erforderlich. Aus diesem Grund konzentriert sich die vorliegende Untersuchung auf die Mechanismen und die Minimierung des Werkzeugverschleißes und die Auswirkungen auf die Oberfläche eines in Kokille vergossenen FeAl-Bauteils. Neben den Optimierungen des Fräsprozesses und der Werkzeugparameter (Geometrie, Material) wird ein modernes hybrides Bearbeitungsverfahren, das ultra-schallunterstützte Fräsen (USAM), eingesetzt, bei dem eine Überlagerung mit einer hochfrequenten Schwingung des rotierenden Werkzeugs erzeugt wird. Analysen der Kräfte und Temperaturen im Fräsprozess, der Verschleißerscheinungen am Werkzeug und der Oberflächenintegrität zeigen positive Auswirkungen durch USAM. Darüber hinaus wird eine valide Grundlage für die Optimierung des Werkzeugs und des Fräsprozesses geschaffen, um eine hohe Oberflächenintegrität (z. B. Verringerung von Zugeigenspannungen und Defekten) und eine längere Werkzeuglebensdauer zu gewährleisten, die zukünftig eine wirtschaftliche Herstellung von FeAl-Bauteilen ermöglicht. T2 - 5. Symposium Materialtechnik CY - Clausthal-Zellerfeld, Germany DA - 23.02.2023 KW - Eisenaluminid KW - Ultraschallunterstütztes Fräsen KW - Werkzeugverschleiß KW - Oberflächenintegrität PY - 2023 VL - 12 SP - 738 EP - 748 PB - Shaker Verlag CY - Düren AN - OPUS4-59219 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Remmler, Dario A1 - Schwaar, Timm A1 - Pickhardt, M. A1 - Donth, C. A1 - Mandelkow, E. A1 - Weller, Michael G. A1 - Börner, H. T1 - On the way to precision formulation additives: 2D-screening to select solubilizers with tailored host and release capabilities N2 - A 2-dimensional high-throughput screening method is presented to select peptide sequences from large peptide libraries for precision formulation additives, having a high capacity to specifically host a drug of interest and provide tailored drug release properties. The identified sequences are conjugated with poly(ethylene glycol) (PEG) to obtain peptide-PEG conjugates that proved to be valuable as solubilizers for small organic molecule drugs to overcome limitations of poor water-solubility and low bio-availability. The 2D-screening method selects peptide sequences on both (i) high loading capacities and (ii) preferred drug-release capabilities as demonstrated on an experimental Tau-protein aggregation inhibitor/Tau- deaggregator with potentials for an anti-Alzheimer disease drug (BB17). To enable 2D-screening, a one-bead one-compound (OBOC) peptide library was immobilized on a glass slide, allocating individual beads to permanent positions. While the first screening step involved incubation of the supported OBOC library with BB17 to identify beads with high drug binding capacities by fluorescence scanner readouts, the second step reveals release properties of the high capacity binders by incubation with blood plasma protein model solutions. Efficiently peptides with high BB17 capacities and either keeper or medium or fast releaser properties can be identified by direct sequence readouts from the glass slide supported resin beads via matrix-assisted laser desorption/ionization time-of-flight tandem mass spectrometry. Four peptides are synthesized as peptide-PEG solubilizers representing strong, medium, weak releasers and non-binders. Loading capacities reached up to 1:3.4 (mol drug per mol carrier) and release kinetics (fast/medium/slow) are in agreement with the selection process as investigated by fluorescence anisotropy and fluorescence correlation spectroscopy. The ability of BB17/conjugate complexes to inhibit the aggregation of Tau4RDΔK (four repeat Tau ((M)Q244-E372 with deletion of K280), 129 residues) in N2a cells is studied by a Tau-pelleting assay showing the modulation of cellular Tau aggregation. Promising effects such as the reduction of 55% of total Tau load are observed for the strong releaser additive. Studies of in vitro Thioflavin S Tau-aggregation assays show half-maximal inhibitory activities (IC50 values) of BB17/conjugates in the low micro-molar range. KW - Block copolymer KW - Drug transporters KW - Peptide library screening KW - Formulation additives PY - 2018 DO - https://doi.org/10.1016/j.jconrel.2018.06.032 SN - 0168-3659 SN - 1873-4995 VL - 285 SP - 96 EP - 105 PB - Elsevier CY - Amsterdam AN - OPUS4-45483 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bauer, M. A1 - Remmler, D. A1 - Dallmann, A. A1 - Jakubowski, Norbert A1 - Börner, H. G. A1 - Panne, Ulrich A1 - Limberg, C. T1 - Specific Decoration of a Discrete Bismuth Oxido Cluster by Selected Peptides towards the Design of Metal Tags N2 - Metal tags find application in a multitude of biomedical systems and the combination with laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) offers an opportunity for multiplexing. To lay the foundation for an increase of the signal intensities in such processes, we herein present a general approach for efficient functionalization of a well-defined metal oxido cluster [Bi6O4(OH)(4)(SO3CF3)(6)(CH3CN)(6)].2 CH3CN (1), which can be realized by selecting 7mer peptide sequences via combinatorial means from large one-bead one-compound peptide libraries. Selective cluster-binding peptide sequences (CBS) for 1 were discriminated from non-binders by treatment with H2S gas to form the reduction product Bi2S3, clearly visible to the naked eye. Interactions were further confirmed by NMR experiments. Extension of a binding peptide with a maleimide linker (Mal) introduces the possibility to covalently attach thiol-bearing moieties such as biological probes and for their analysis the presence of the cluster instead of mononuclear entities should lead to an increase of signal intensities in LA-ICP-MS measurements. To prove this, CBS-Mal was covalently bound onto thiol-presenting glass substrates, which then captured 1 effectively, so that LA-ICP-MS measurements demonstrated drastic signal amplification compared to single lanthanide tags. KW - Peptide library KW - Mass spectrometry KW - Laser ablation KW - Cluster KW - Bioconjugation PY - 2019 DO - https://doi.org/10.1002/chem.201805234 SN - 0947-6539 VL - 25 IS - 3 SP - 759 EP - 763 PB - John Wiley & Sons, Inc. AN - OPUS4-47324 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Schwaar, Timm A1 - Lettow, Maike A1 - Remmler, Dario A1 - Börner, H. G. A1 - Weller, Michael G. T1 - Efficient Screening of Combinatorial Peptide Libraries by Spatially Ordered Beads Immobilized on Conventional Glass Slides N2 - Screening of one-bead-one-compound (OBOC) libraries is a proven procedure for the identification of protein-binding ligands. The demand for binders with high affinity and specificity towards various targets has surged in the biomedical and pharmaceutical field in recent years. The traditional peptide screening involves tedious steps such as affinity selection, bead picking, sequencing, and characterization. Herein, we present a high-throughput “all-on-one chip” system to avoid slow and technically complex bead picking steps. On a traditional glass slide provided with an electrically conductive tape, beads of a combinatorial peptide library are aligned and immobilized by application of a precision sieve. Subsequently, the chip is incubated with a fluorophore-labeled target protein. In a fluorescence scan followed by matrix-assisted laser desorption/ionization (MALDI)-time of flight (TOF) mass spectrometry, high-affinity binders are directly and unambiguously sequenced with high accuracy without picking of the positive beads. The use of an optimized ladder sequencing approach improved the accuracy of the de-novo sequencing step to nearly 100%. The new technique was validated by employing a FLAG-based model system, identifying new peptide binders for the monoclonal M2 anti-FLAG antibody, and was finally utilized to search for IgG-binding peptides. In the present format, more than 30,000 beads can be screened on one slide. KW - Peptide library KW - HTS KW - Target KW - MALDI KW - Mass spectrometry KW - Biochip KW - Lab-on-a-Chip KW - Array KW - Screening KW - Ladder sequencing KW - Binder KW - Pharmaceutical PY - 2019 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-478973 UR - https://www.mdpi.com/2571-5135/8/2/11 DO - https://doi.org/10.3390/ht8020011 VL - 8 IS - 2 SP - 1 EP - 15 PB - MDPI CY - Basel AN - OPUS4-47897 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Celasun, S. A1 - Remmler, D. A1 - Schwaar, Timm A1 - Weller, Michael G. A1 - Du Prez, F. A1 - Börner, H. G. T1 - Digging into the sequential space of thiolactone precision polymers: A combinatorial strategy to identify functional domains N2 - Functional sequences of precision polymers based on thiolactone/Michael chemistry are identified from a large one-bead one-compound library. Single-bead readout by MALDI-TOF MS/MS identifies sequences that host m-THPC that is a second Generation photo-sensitizer drug. The corresponding Tla/Michael-PEG conjugates make m-THPC available in solution and drug payload as well as drug release kinetics can be fine-tuned by the precision segment. KW - Combinatorial chemistry KW - Combinatorial polymer libraries KW - Sequence-defined oligomer KW - Precision polymer sequencing KW - Pseudo peptides KW - MALDI-TOF KW - ESI MS KW - Mass spectrometry KW - Sequencing KW - PEG KW - Polyethylene glycol KW - Solubilizer KW - Drug KW - Conjugates PY - 2019 DO - https://doi.org/10.1002/anie.201810393 SN - 1521-3773 VL - 58 IS - 7 SP - 1960 EP - 1964 PB - Wiley-VCH CY - Weinheim AN - OPUS4-47323 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Wieczorek, S. A1 - Schwaar, Timm A1 - Senge, M. O. A1 - Börner, H.G. T1 - Specific drug formulation additives: Revealing the impact of architecture and block length ratio N2 - Combining poly(ethylene glycol) (PEG) with sequence-defined peptides in PEG–peptide conjugates offers opportunities to realize next-generation drug formulation additives for overcoming undesired pharmacological profiles of difficult small molecule drugs. The tailored peptide segments provide sequence-specific, noncovalent drug binding, and the hydrophilic PEG block renders the complexes water soluble. On the basis of a peptide sequence known to bind the photosensitizer m-tetra(hydroxyphenyl)chlorin (m-THPC) for photodynamic cancer therapy, a set of different conjugate architectures is synthesized and studied. Variations in PEG block length and amplification of the peptidic binding domain of PEG–peptide conjugates are used to fine tune critical parameters for hosting m-THPC, such as drug payload capacities, aggregation sizes, and drug release and activation kinetics. PY - 2015 DO - https://doi.org/10.1021/acs.biomac.5b00961 SN - 1525-7797 VL - 16 IS - 10 SP - 3308 EP - 3312 PB - ACS Publ. CY - Washington, DC, USA AN - OPUS4-35037 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Stutz, C. A1 - Bilecka, I. A1 - Thünemann, Andreas A1 - Niederberger, M. A1 - Börner, H.G. T1 - Superparamagnetic core-shell nanoparticles as solid supports for peptide synthesis N2 - Functional superparamagnetic core–shell nanoparticles are synthesized by a microwave assisted route and can be used as colloidal supports for peptide synthesis in 'quasi solution'. KW - Nanotechnology KW - Small-angle X-ray scatering KW - SAXS PY - 2012 DO - https://doi.org/10.1039/c2cc33492e SN - 0022-4936 SN - 0009-241x SN - 1359-7345 SN - 1364-548x VL - 48 IS - 57 SP - 7176 EP - 7178 PB - Royal Society of Chemistry CY - Cambridge AN - OPUS4-26116 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -