Proteomics methods for subcellular proteome analysis

被引:80
作者
Drissi, Romain [1 ]
Dubois, Marie-Line [1 ]
Boisvert, Francois-Michel [1 ]
机构
[1] Univ Sherbrooke, Dept Anat & Cell Biol, Sherbrooke, PQ J1E 4K8, Canada
基金
加拿大健康研究院;
关键词
MS; organelle; proteomics; stable isotope labeling by amino acids in cell culture (SILAC); subcellular compartment; MASS-SPECTROMETRY; ORGANELLE PROTEINS; LOCALIZATION; IDENTIFICATION; FRACTIONATION; COMPLEX; ELECTROPHORESIS; PEROXISOMES; EXPRESSION; RESOLUTION;
D O I
10.1111/febs.12502
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The elucidation of the subcellular distribution of proteins under different conditions is a major challenge in cell biology. This challenge is further complicated by the multicompartmental and dynamic nature of protein localization. To address this issue, quantitative proteomics workflows have been developed to reliably identify the protein complement of whole organelles, as well as for protein assignment to subcellular location and relative protein quantification based on different cell culture conditions. Here, we review quantitative MS-based approaches that combine cellular fractionation with proteomic analysis. The application of these methods to the characterization of organellar composition and to the determination of the dynamic nature of protein complexes is improving our understanding of protein functions and dynamics.
引用
收藏
页码:5626 / 5634
页数:9
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