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Protein-Protein Interaction Detection Via Mass Spectrometry-Based Proteomics

机译:蛋白质 - 蛋白质相互作用检测通过质谱基蛋白质组学检测

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摘要

Analysis of protein-protein interactions is one of the mainstays of mass spectrometry-based proteomics and recent developments, which have simplified the methodology, have permitted non-specialised laboratories to adopt the approach. We introduce and review three complimentary methods which allow for the targeted, global and site-specific analysis of protein complexes. Co-precipitation of endogenous or ectopically expressed proteins and their complexes followed by proteomic analysis allows for the discovery and accurate quantification of specific protein interactions. Whereas complimentary methods, such as co-purification of entire complexes based on physico-chemical attributes, can give a snapshot of the composition and dynamics of protein complexes on a global scale. Cross-linking on the other hand can pinpoint the amino acids involved in protein-protein interactions to such a resolution that the likely complex can be reconstructed computationally.
机译:蛋白质 - 蛋白质相互作用的分析是大众光谱法的蛋白质组学的主体之一,最近的发展简化了方法,允许非专业化实验室采用这种方法。 我们介绍和审查三种允许针对蛋白质复合物的目标,全球和网站特异性分析的三种补充方法。 内源性或异位表达蛋白质的共沉淀及其复合物,然后进行蛋白质组学分析,允许发现和准确地定量特定的蛋白质相互作用。 虽然根据物理化学属性,如整个复合物的共同纯化的互补方法,可以在全球范围内给出蛋白质复合物的组成和动态的快照。 另一方面,交联可以针对蛋白质 - 蛋白质相互作用的氨基酸定位,这是可能的复合物可以计算地重建。

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