The use of isotope-coded affinity tags (ICAT) to study organelle proteomes in Arabidopsis thaliana

被引:40
作者
Dunkley, TPJ
Dupree, P
Watson, RB
Lilley, KS
机构
[1] Univ Cambridge, Dept Biochem, Cambridge Ctr Proteom, Cambridge CB2 1QW, England
[2] Appl Biosyst Inc, Warrington WA3 7QH, Cheshire, England
基金
英国生物技术与生命科学研究理事会;
关键词
Golgi; isotope-coded affinity tag (ICAT); membrane protein; organelle; quantitative proteonomics;
D O I
10.1042/BST0320520
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
Organelle proteomics is the analysis of the protein contents of a subcellular compartment. Proteins identified in subcellular proteomic studies can only be assigned to an organelle if there are no contaminants present in the sample preparation. As a result, the majority of plant organelle proteomic studies have focused on the chloroplast and mitochondria, which can be isolated relatively easily. However, the isolation of components of the endomembrane system is far more difficult due to their similar sizes and densities. For this reason, quantitative proteomics methods are being developed to enable the assignment of proteins to a specific component of the endomembrane system without the need to obtain pure organelles.
引用
收藏
页码:520 / 523
页数:4
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