Chemical Tools to Study Protein ADP-Ribosylation

被引:10
|
作者
van Noort, Gerbrand J. van der Heden [1 ]
机构
[1] Leiden Univ, Med Ctr, Dept Cell & Chem Biol, NL-2333 ZC Leiden, Netherlands
来源
ACS OMEGA | 2020年 / 5卷 / 04期
关键词
NAD(+) ANALOGS; RIBOSE; ADENOSINE; SERINE;
D O I
10.1021/acsomega.9b03591
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Post-translational modification of substrate proteins plays crucial roles in the regulation of their activity, cellular localization, and ability to be recognized by other proteins. One of those modifications involves the installment of adenosine-diphosphate-ribose (ADPr) onto nucleophilic side-chain groups of amino acid residues. This highly dynamic process is regulated by ADP-ribosyl transferases (ARTs) that install the ADPr-molecules on selected proteins and poly(ADP-ribosyl) glycohydrolases (PARGs) and (ADP-ribosyl) hydrolases (ARHs) that trim down and remove ADPr-chains. In this mini-review, the most recent advances in the chemical synthesis of ADPr-conjugates, poly-ADP-ribose, ADPr-peptides, and -proteins, and other tools to investigate ADPr-biology are discussed.
引用
收藏
页码:1743 / 1751
页数:9
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