TY - JOUR A1 - Polatajko, A. A1 - Feldmann, I. A1 - Hayen, H. A1 - Jakubowski, Norbert T1 - Combined application of a laser ablation-ICP-MS assay for screening and ESI-FTICR-MS for identification of a Cd-binding protein in Spinacia oleracea L. after exposure to Cd JF - Metallomics N2 - We have studied the binding of the toxic element Cd to plant proteins and have used for this purpose spinach (Spinacia oleracea L.) plants treated with 50 µM Cd(II) as a model system. Laser ablation ICP-MS has been applied for the screening of Cd-binding proteins after separation by native anodal polyacrylamide gel electrophoresis (AN-PAGE) and electroblotting onto membranes. The main Cd-carrying protein band was isolated and investigated by nano-electrospray ionization–Fourier transform ion cyclotron resonance (FTICR) mass spectrometry after tryptic digestion. By this procedure, the main Cd-binding protein was identified as ribulose-1,5-bisphosphate carboxylase/oxygenase (RuBisCO). The latter enzyme has been discussed in the literature to be affected in its activity by oxidative stress induced by Cd. However, in this paper it is demonstrated for the first time that RuBisCO directly binds Cd and thus may be directly altered by this toxic element. A commercially available protein standard was used to verify direct binding of Cd(II) to the protein, even without metabolisation. The resulting metal–protein complex was shown to be stable enough to survive AN-PAGE separation and electroblotting. By the use of size exclusion chromatography coupled with ICP-MS it was demonstrated that the RuBisCO protein standard shows similar metal binding properties to Cd. Furthermore, essential elements such as Mn(II), Fe(II) and Cu(II), which are known to possibly replace the RuBisCO activator Mg(II), were investigated in addition to Zn(II). Again, similar binding properties in comparison to the plant protein were observed. PY - 2011 DO - https://doi.org/10.1039/c1mt00051a SN - 1756-5901 SN - 1756-591X VL - 3 IS - 10 SP - 1001 EP - 1008 PB - RSC Publ. CY - Cambridge AN - OPUS4-24963 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Müller, Larissa A1 - Jakubowski, Norbert A1 - Hayen, H. A1 - Roos, P.H. T1 - Iodination of proteins, proteomes and antibodies with potassium triodide for LA-ICP-MS based proteomic analyses JF - Journal of analytical atomic spectrometry N2 - A fast and mild method for iodine labelling of proteins is presented which is specifically designed and optimized for laser ablation (LA-)ICP-MS based proteomics. Single proteins (lysozyme, bovine serum albumin, cytochrome c and β-casein), whole proteomes (microsomal proteome of rats) and antibodies (anti-bovine casein, anti-bovine serum albumin) can be efficiently iodinated by means of potassium triiodide with minimal losses of antigen properties and antibody binding to iodinated proteins. A comparison with iodination by use of IODO-Beads is presented and it is shown that triiodide labelling is a fast, cheap and less laborious alternative without compromising the analytical figures of merit. PY - 2011 DO - https://doi.org/10.1039/c1ja10090d SN - 0267-9477 SN - 1364-5544 N1 - Geburtsname von Müller, Larissa: Wäntig, L. - Birth name of Müller, Larissa: Wäntig, L. VL - 26 SP - 1610 EP - 1618 PB - Royal Society of Chemistry CY - London AN - OPUS4-24209 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Maiwald, Michael A1 - Sperling, M. A1 - Huber, C. A1 - Hayen, H. A1 - Teutenberg, T. A1 - Belder, D. A1 - Karst, U. A1 - Hagenhoff, B. A1 - Vogel, M. T1 - Prozessanalytik: Spektroskopie und Miniaturisierung JF - Trendbericht Analytische Chemie 2014/2015 N2 - Forderungen nach höherer Geschwindigkeit und die Komplexität der Fragen geben der analytischen Chemie neue Impulse. So nutzt die Prozessanalytik gepulste Ramanspektrometer, die Elemente Arsen und Quecksilber dominieren die Forschung in der Speziesanalytik, und die Omics-Techniken entwickeln sich zu Multi-Omics-Ansätzen. Ambiente MS-Techniken benötigen keine aufwendige Probenvorbereitung, multidimensionale Trenntechniken werden verstärkt in der Routine eingesetzt, und Chip-basierte Trennungen fallen durch Schnelligkeit auf. Molekülspektroskopie und Massenspektrometrie dominieren die bildgebenden Verfahren, und die Lateralauflösung der ToF-Sekundärionenmassenspektrometrie hat sich bei Oberflächenuntersuchungen verbessert. KW - Prozessanalytik KW - Quanten-Kaskadenlaser KW - Photonendichtewellen-Spektroskopie KW - Gepulste Ramanspektrometer KW - Partikelmesstechnik KW - Prozesssensoren PY - 2016 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-361371 UR - http://onlinelibrary.wiley.com/doi/10.1002/nadc.20164046080/abstract DO - https://doi.org/10.1002/nadc.20164046080 SN - 1868-0054 VL - 64 IS - 5 SP - 497 EP - 508 PB - Wiley-VCH Verlag GmbH & Co. KGaA CY - Weinheim AN - OPUS4-36137 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Hayen, H. A1 - Polatajko, A. A1 - Feldmann, I. A1 - Jakubowski, Norbert T1 - Identifizierung Cadmium-bindender Proteine in Spinat T2 - Jahrestagung des Regionalverbandes Nordrhein-Westfalen der Lebensmittelchemischen Gesellschaft (Fachgruppe der GDCh) T2 - Jahrestagung des Regionalverbandes Nordrhein-Westfalen der Lebensmittelchemischen Gesellschaft (Fachgruppe der GDCh) CY - Wuppertal, Germany DA - 2011-03-23 PY - 2011 AN - OPUS4-23824 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -