Abstract
Histone lysine acetyltransferases (KATs) catalyze the transfer of the acetyl group from acetyl Coenzyme A to lysine residues in histones and nonhistone proteins. Here, we report biomolecular studies on epigenetic acetylation and related acylation reactions of lysine and γ-thialysine, a cysteine-derived lysine mimic, which can be site-specifically introduced to histone peptides and histone proteins. Enzyme assays demonstrate that human KATs catalyze an efficient acetylation and propionylation of histone peptides that possess lysine and γ-thialysine. Enzyme kinetics analyses reveal that lysine- and γ-thialysine-containing histone peptides exhibit indistinguishable Km values, whereas small differences in kcat values were observed. This work highlights that γ-thialysine may act as a representative and easily accessible lysine mimic for chemical and biochemical examinations of post-translationally modified histones.
| Originalsprog | Engelsk |
|---|---|
| Tidsskrift | Bioconjugate Chemistry |
| Vol/bind | 31 |
| Udgave nummer | 3 |
| Sider (fra-til) | 844-851 |
| ISSN | 1043-1802 |
| DOI | |
| Status | Udgivet - 18. mar. 2020 |
Fingeraftryk
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