Saghatelian Alan, Cravatt Benjamin F
The Skaggs Institute for Chemical Biology, Departments of Cell Biology and Chemistry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
Curr Opin Chem Biol. 2005 Feb;9(1):62-8. doi: 10.1016/j.cbpa.2004.12.004.
A fundamental goal of proteomics is to assign physiological functions to all proteins encoded by eukaryotic and prokaryotic genomes. Of the many activities performed by proteins, the chemical transformations catalyzed by enzymes form the basis for most, if not all, metabolic and signaling pathways. Elucidation of these pathways and their integration into larger cellular networks require new strategies to rapidly and systematically identify physiological substrates of enzymes. Here, we review emerging technologies that aim to assign endogenous biochemical functions to enzymes by profiling the metabolome.
蛋白质组学的一个基本目标是为真核生物和原核生物基因组编码的所有蛋白质赋予生理功能。在蛋白质执行的众多活动中,酶催化的化学转化构成了大多数(即便不是全部)代谢和信号通路的基础。阐明这些通路并将它们整合到更大的细胞网络中,需要新的策略来快速且系统地鉴定酶的生理底物。在此,我们综述旨在通过对代谢组进行分析来赋予酶内源性生化功能的新兴技术。