High throughput strategies for probing the different organizational levels of protein interaction networks

被引:10
|
作者
Kristensen, Anders R. [1 ]
Foster, Leonard J. [1 ]
机构
[1] Univ British Columbia, Ctr High Throughput Biol, Dept Biochem & Mol Biol, Vancouver, BC V5Z 1M9, Canada
关键词
CHEMICAL CROSS-LINKING; MASS-SPECTROMETRY; QUANTITATIVE PROTEOMICS; MULTIPROTEIN COMPLEXES; BAC TRANSGENEOMICS; ORGANELLE PROTEINS; GLOBAL LANDSCAPE; LINKED PEPTIDES; GENOME-WIDE; IDENTIFICATION;
D O I
10.1039/c3mb70135b
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Most proteins do not exist as isolated molecules in the cell, but instead serve as nodes of protein interaction networks. A number of techniques have been developed in the last two decades to study protein interaction networks at different levels of detail. Here we describe some of the techniques for characterizing protein interactions and protein complexes on a system-wide scale, focusing especially on newly emerging techniques that use co-migration. These newer approaches have the advantage that no genetic manipulation is necessary, thereby allowing investigation of protein complexes at their endogenous levels in the correct cellular context. Finally, we discuss different approaches for measuring large-scale temporal changes to protein interaction networks, an area that we believe will be one of the frontiers in systems biology in the coming years.
引用
收藏
页码:2201 / 2212
页数:12
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