Methyltransferase-Directed Labeling of Biomolecules and its Applications

被引:62
作者
Deen, Jochem [1 ]
Vranken, Charlotte [2 ]
Leen, Volker [2 ]
Neely, Robert K. [3 ]
Janssen, Kris P. F. [2 ]
Hofkens, Johan [2 ]
机构
[1] Ecole Polytech Fed Lausanne, Lab Nanoscale Biol, Sch Engn, STI IBI STI LBEN, BM 5134,Batiment BM,Stn 17, CH-1015 Lausanne, Switzerland
[2] Katholieke Univ Leuven, Dept Chem, Lab Photochem & Spect, Celestijnenlaan 200F, B-3001 Heverlee, Belgium
[3] Univ Birmingham, Sch Chem, Birmingham B15 2TT, W Midlands, England
基金
欧洲研究理事会; 英国工程与自然科学研究理事会;
关键词
S-adenosyl methionine; DNA functionalization; methyltransferases; protein modification; transalkylation; ADENOSYL-L-METHIONINE; S-ADENOSYLMETHIONINE SYNTHETASE; N-MUSTARD ANALOGS; PROTEIN ARGININE METHYLATION; DNA METHYLTRANSFERASE; SINGLE-MOLECULE; CHEMOENZYMATIC SYNTHESIS; ESCHERICHIA-COLI; COFACTOR ANALOG; ADOMET ANALOG;
D O I
10.1002/anie.201608625
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Methyltransferases (MTases) form a large family of enzymes that methylate a diverse set of targets, ranging from the three major biopolymers to small molecules. Most of these MTases use the cofactor S-adenosyl-l-Methionine (AdoMet) as a methyl source. In recent years, there have been significant efforts toward the development of AdoMet analogues with the aim of transferring moieties other than simple methyl groups. Two major classes of AdoMet analogues currently exist: doubly-activated molecules and aziridine based molecules, each of which employs a different approach to achieve transalkylation rather than transmethylation. In this review, we discuss the various strategies for labelling and functionalizing biomolecules using AdoMet-dependent MTases and AdoMet analogues. We cover the synthetic routes to AdoMet analogues, their stability in biological environments and their application in transalkylation reactions. Finally, some perspectives are presented for the potential use of AdoMet analogues in biology research, (epi)genetics and nanotechnology.
引用
收藏
页码:5182 / 5200
页数:19
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