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一锅法、光控酶组装结构定义的异源多聚泛素链。

One-Pot, Photocontrolled Enzymatic Assembly of the Structure-Defined Heterotypic Polyubiquitin Chain.

机构信息

Department of Chemistry and Biotechnology, Graduate School of Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656, Japan.

Department of Advanced Interdisciplinary Studies, Graduate School of Engineering, The University of Tokyo, 4-6-1 Komaba, Meguro-ku, Tokyo 153-8904, Japan.

出版信息

J Am Chem Soc. 2023 May 31;145(21):11690-11700. doi: 10.1021/jacs.3c01912. Epub 2023 May 18.

Abstract

Heterotypic polyubiquitins are an emerging class of polyubiquitins that have attracted interest because of their potential diversity of structures and physiological functions. There is an increasing demand for structure-defined synthesis of heterotypic chains to investigate the topological factors underlying the intracellular signals that are characteristically mediated by the heterotypic chain. However, the applicability of chemical and enzymatic polyubiquitin synthesis developed to date has been limited by laborious rounds of ligation and purification or by a lack of modularity of the chain structure with respect to the length and the branch position. Here, we established a one-pot, photocontrolled synthesis of structurally defined heterotypic polyubiquitin chains. We designed ubiquitin derivatives with a photolabile protecting group at a lysine residue used for polymerization. Repetitive cycles of linkage-specific enzymatic elongation and photoinduced deprotection of the protected ubiquitin units enabled stepwise addition of ubiquitins with appropriate functionalities to control the length and branching positions. The positional control of branching was achieved without isolation of intermediates, allowing one-pot synthesis of K63 triubiqutin chains and a K63/K48 heterotypic tetraubiquitin chain with defined branching positions. The present study provides a chemical platform for the efficient construction of long polyubiquitin chains with defined branch structures that will facilitate the understanding of the essential relationships between functions and structures of the heterotypic chain that have hitherto been overlooked.

摘要

杂合多聚泛素是一类新兴的多聚泛素,由于其结构和生理功能的多样性而引起了人们的兴趣。人们越来越需要对杂合链进行结构定义的合成,以研究由杂合链介导的细胞内信号的拓扑因素。然而,迄今为止开发的化学和酶法多聚泛素合成的适用性受到繁琐的连接和纯化循环或链结构相对于长度和分支位置的模块化的限制。在这里,我们建立了一种一锅法、光控合成结构定义的杂合多聚泛素链的方法。我们设计了带有赖氨酸残基上光不稳定保护基团的泛素衍生物,用于聚合。通过连接特异性酶促延伸和受保护的泛素单元的光诱导脱保护的重复循环,能够逐步添加具有适当功能的泛素,以控制长度和分支位置。分支的位置控制是在不分离中间体的情况下实现的,从而允许一锅法合成 K63 三泛素链和具有定义分支位置的 K63/K48 杂合四泛素链。本研究为具有定义分支结构的长多聚泛素链的高效构建提供了一个化学平台,这将有助于理解迄今为止被忽视的杂合链的功能和结构之间的基本关系。

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