High-throughput fluorescence microscopic analysis of protein abundance and localization in budding yeast

被引:10
|
作者
Torres, Nikko P.
Ho, Brandon
Brown, Grant W. [1 ,2 ]
机构
[1] Univ Toronto, Dept Biochem, Room 1206,160 Coll St, Toronto, ON M5S 3E1, Canada
[2] Univ Toronto, Donnelly Ctr, Room 1206,160 Coll St, Toronto, ON M5S 3E1, Canada
基金
加拿大健康研究院; 加拿大自然科学与工程研究理事会;
关键词
genomics; protein abundance; yeast; Fluorescence microscopy; protein localization; quantitative cell biology; STOCHASTIC GENE-EXPRESSION; INNER NUCLEAR-MEMBRANE; DNA-DAMAGE RESPONSE; GENOME-WIDE SCREEN; SACCHAROMYCES-CEREVISIAE; SINGLE-CELL; MASS-SPECTROMETRY; ENVIRONMENTAL-CHANGES; GLOBAL ANALYSIS; QUALITY CONTROL;
D O I
10.3109/10409238.2016.1145185
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
Proteins directly carry out and regulate cellular functions. As a result, changes in protein levels within a cell directly influence cellular processes. Similarly, it is intuitive that the intracellular localization of proteins is a key component of their functionality. Optimal activity is achieved by a combination of protein concentration, co-compartmentalization with substrates, co-factors and regulators and sequestration from deleterious locales. The proteome within a cell is highly dynamic and changes in response to different environmental conditions. High-throughput microscopic analysis in the budding yeast Saccharomyces cerevisiae has afforded proteome-wide views of protein organization in living cells, and of how protein abundance and location is regulated and remodeled in response to stress.
引用
收藏
页码:110 / 119
页数:10
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