| Literature DB >> 35302274 |
Yusheng Xie1, Shubo Du2, Zhiyang Liu3, Min Liu1, Zhiqiang Xu3, Xiaojie Wang1, Jia Xuan Kee2, Fan Yi1, Hongyan Sun3, Shao Q Yao2.
Abstract
Lysine acylation plays pivotal roles in cell physiology, including DNA transcription and repair, signal transduction, immune defense, metabolism, and many other key cellular processes. Molecular mechanisms of dysregulated lysine acylation are closely involved in the pathophysiological progress of many human diseases, most notably cancers. In recent years, chemical biology tools have become instrumental in studying the function of post-translational modifications (PTMs), identifying new "writers", "erasers" and "readers", and in targeted therapies. Here, we describe key developments in chemical biology approaches that have advanced the study of lysine acylation and its regulatory proteins (2016-2021). We further discuss the discovery of ligands (inhibitors and PROTACs) that are capable of targeting regulators of lysine acylation. Next, we discuss some current challenges of these chemical biology probes and suggest how chemists and biologists can utilize chemical probes with more discriminating capacity. Finally, we suggest some critical considerations in future studies of PTMs from our perspective.Entities:
Keywords: Chemical Probes; Epigenetics; Lysine Acylation; PROTAC; Protein Machinery
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Year: 2022 PMID: 35302274 DOI: 10.1002/anie.202200303
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336