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使用免疫共沉淀和质谱技术鉴定秀丽隐杆线虫中的蛋白质复合物组分。

Identifying components of protein complexes in C. elegans using co-immunoprecipitation and mass spectrometry.

机构信息

Department of Chemical Physiology, The Scripps Research Institute, La Jolla, California 92037, USA.

出版信息

J Proteomics. 2010 Oct 10;73(11):2198-204. doi: 10.1016/j.jprot.2010.05.008. Epub 2010 May 28.

Abstract

Mass spectrometry-based proteomics is rapidly becoming an essential tool for biologists. One of the most common applications is identifying the components of protein complexes isolated by co-immunoprecipitation. In this review, we discuss the co-immunoprecipitation, mass spectrometry and data analysis techniques that have been used successfully to define protein complexes in C. elegans research. In this discussion, two strategies emerged. One approach is to use stringent biochemical purification methods and attempt to identify a small number of complex components with a high degree of certainty based on MS data. A second approach is to use less stringent purification and identification parameters, and ultimately test a longer list of potential binding partners in biological validation assays. This should provide a useful guide for biologists planning proteomic experiments.

摘要

基于质谱的蛋白质组学正在迅速成为生物学家的重要工具。其中最常见的应用之一是鉴定通过免疫共沉淀分离的蛋白质复合物的组成成分。在这篇综述中,我们讨论了已成功用于定义秀丽隐杆线虫研究中蛋白质复合物的免疫共沉淀、质谱和数据分析技术。在这一讨论中,出现了两种策略。一种方法是使用严格的生化纯化方法,并尝试根据 MS 数据以高度确定性鉴定少数复杂成分。另一种方法是使用不那么严格的纯化和鉴定参数,并最终在生物验证实验中测试更长的潜在结合伙伴列表。这应该为计划蛋白质组学实验的生物学家提供有用的指导。

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