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使用不可逆分选酶介导的连接进行具有位点特异性修饰的组蛋白H4半合成方案。

Protocol for semisynthesis of histone H4 with site-specific modifications using irreversible sortase-mediated ligation.

作者信息

Xiao Yihang, Zou Kun, Wu Mingxuan

机构信息

Department of Chemistry, School of Science, Westlake University, Hangzhou, Zhejiang Province 310030, China; Institute of Natural Sciences, Westlake Institute for Advanced Study, Hangzhou, Zhejiang Province 310024, China.

Department of Chemistry, School of Science, Westlake University, Hangzhou, Zhejiang Province 310030, China.

出版信息

STAR Protoc. 2025 Mar 21;6(1):103527. doi: 10.1016/j.xpro.2024.103527. Epub 2025 Jan 3.

Abstract

Post-translational modifications (PTMs) of histone H4 play significant roles in the regulation of chromatin status. Here, we present a protocol for semisynthesis of histone H4 by sortase-mediated ligation (SML). We describe steps for solid-phase peptide synthesis of H4R40C(1-42), recombinant expression and purification of H4(41-102), expression and purification of eSrt(2A-9), and preparation of acrylamidine. We then detail procedures for SML of histone H4. This protocol can also be applied to the preparation of homogenous proteins with PTMs. For complete details on the use and execution of this protocol, please refer to Xiao et al..

摘要

组蛋白H4的翻译后修饰(PTM)在染色质状态调节中发挥着重要作用。在此,我们展示了一种通过分选酶介导的连接(SML)进行组蛋白H4半合成的方案。我们描述了H4R40C(1 - 42)的固相肽合成、H4(41 - 102)的重组表达与纯化、eSrt(2A - 9)的表达与纯化以及丙烯脒制备的步骤。然后我们详细说明了组蛋白H4的SML程序。该方案也可应用于具有PTM的同源蛋白的制备。有关此方案使用和执行的完整详细信息,请参考Xiao等人的文献。

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