4.6 Article

Genetically Encoded Benzoyllysines Serve as Versatile Probes for Interrogating Histone Benzoylation and Interactions in Living Cells

期刊

ACS CHEMICAL BIOLOGY
卷 16, 期 11, 页码 2560-2569

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acschembio.1c00614

关键词

-

资金

  1. National Science Foundation of China (NSFC) [21778062, 92053106]
  2. Science and Technology Commission of Shanghai Municipality, China [18431907100]
  3. ShanghaiTech University
  4. Analytical Instrumentation Center at ShanghaiTech University [SPSTAIC10112914]

向作者/读者索取更多资源

This study presents a novel approach to genetically encode benzoyllysine and fluorinated benzoyllysines into full-length histone proteins in a site-specific manner in live cells. The incorporated unnatural amino acids allow for versatile probes to investigate histone benzoylation under biological environments, providing multiple signals such as F-19 NMR spectra with chemical clarity and fluorescence signals.
Histone posttranslational modifications (PTMs) are vital epigenetic regulators in many fundamental cell signaling pathways and diverse biological processes. Histone lysine benzoylation is a recently identified epigenetic mark associated with active transcription; however, it remains to be explored. Herein, we first report the genetic encoding of benzoyllysine and fluorinated benzoyllysines into full-length histone proteins in a site-specific manner in live cells, based on our rationally designed synthetase and fine-integrated fluorine element into benzoyllysines. The incorporated unnatural amino acids integrating unique features were demonstrated as versatile probes for investigating histone benzoylation under biological environments, conferring multiplex signals such as F-19 NMR spectra with chemical clarity and fluorescence signals for benzoylation. Moreover, the site specifically incorporated lysine benzoylation within native full-length histone proteins revealed distinct dynamics of debenzoylation in the presence of debenzoylase sirtuin 2 (SIRT2). Our developed strategy for genetic encoding of benzoyllysines offers a general and novel approach to gain insights into interactions of site-specific histone benzoylation modifications with interactomes and molecular mechanisms in physiological settings, which could not be accessible with fragment histone peptides. This versatile chemical tool enables a direct and new avenue to explore benzoylation, interactions, and histone epigenetics, which will provide broad utilities in chemical biology, protein science, and basic biology research.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据