| Literature DB >> 33467728 |
Giordano Proietti1,2, Yali Wang2,3, Chiara Punzo1, Jasmin Mecinović1,2.
Abstract
Biomedically important histone lysine acetyltransferase KAT8 catalyses the acetyl coenzyme A-dependent acetylation of lysine on histone and other proteins. Here, we explore the ability of human KAT8 to catalyse the acetylation of histone H4 peptides possessing lysine and its analogues at position 16 (H4K16). Our synthetic and enzymatic studies on chemically and structurally diverse lysine mimics demonstrate that KAT8 also has a capacity to acetylate selected lysine analogues that possess subtle changes on the side chain and main chain. Overall, this work highlights that KAT8 has a broader substrate scope beyond natural lysine, and contributes to the design of new chemical probes targeting KAT8 and other members of the histone lysine acetyltransferase (KAT) family.Entities:
Keywords: acetylation; epigenetics; histone; lysine; posttranslational modifications
Mesh:
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Year: 2021 PMID: 33467728 PMCID: PMC7830570 DOI: 10.3390/ijms22020846
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923