Current Chemical Biology Approaches to Interrogate Protein Methyltransferases

被引:107
|
作者
Luo, Minkui [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Mol Pharmacol & Chem Program, New York, NY 10065 USA
关键词
ADENOSYL-L-METHIONINE; ARGININE-METHYLTRANSFERASE; LYSINE METHYLTRANSFERASE; METHYL-LYSINE; AMINO-ACIDS; POSTTRANSLATIONAL MODIFICATIONS; NONHISTONE PROTEINS; KINETIC-ANALYSIS; STRUCTURAL BASIS; ACTIVITY ASSAY;
D O I
10.1021/cb200519y
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
Protein methyltransferases (PMTs) play various physiological and pathological roles through methylating histone and nonhistone targets. However, most PMTs including more than 60 human PMTs remain to be fully characterized. The current approaches to elucidate the functions of PMTs have been diversified by many emerging chemical biology technologies. This review focuses on progress in these aspects and is organized into four discussion modules (assays, substrates, cofactors, and inhibitors) that are important to elucidate biological functions of PMTs. These modules are expected to provide general guidance and present emerging methods for researchers to select and combine suitable PMT-activity assays, well-defined substrates, novel SAM surrogates, and PMT inhibitors to interrogate PMTs.
引用
收藏
页码:443 / 463
页数:21
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