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Quantitative 3D Proteomics Reveals Protein Conformation Changes Using Isotope-labelled Cross-linkers

机译:定量3D蛋白质组学显示使用同位素标记的交联剂揭示蛋白质构象变化

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3D proteomics, a combination of chemical cross-linking, mass spectrometry and database searching, has been increasingly successful in providing medium resolution data on static protein structures. This has been shown by our lab analysing 0.5 MDa and 0.7 MDa Pol II complexes and also by other labs. Integrating quantitation with 3D proteomics promises to provide insights into the structural dynamics of proteins. Here we demonstrate the possibility of using isotope-labelled cross-linkers for quantitation, a strategy that focuses quantitation on cross-linker containing species and places minimal restriction on the protein source.
机译:3D蛋白质组学,化学交联,质谱和数据库搜索的组合在提供了静态蛋白质结构上的中等分辨率数据时越来越成功。这已由我们的实验室显示0.5 MDA和0.7 MDA Pol II复合物以及其他实验室。将定量与3D蛋白质组学集成有望提供蛋白质结构动态的见解。在这里,我们证明了使用同位素标记的交联剂进行定量的可能性,该策略集定量对含有物种的交联剂和对蛋白质来源的最小限制来说。

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