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蛋白质连环体的细胞合成

Cellular Synthesis of Protein Catenanes.

作者信息

Wang Xiao-Wei, Zhang Wen-Bin

机构信息

Key Laboratory of Polymer Chemistry & Physics of Ministry of Education, Center for Soft Matter Science and Engineering, College of Chemistry and Molecular Engineering, Peking University, Beijing, 100871, P.R. China.

出版信息

Angew Chem Int Ed Engl. 2016 Mar 1;55(10):3442-6. doi: 10.1002/anie.201511640. Epub 2016 Feb 2.

Abstract

Direct cellular production of topologically complex proteins is of great interest both in supramolecular chemistry and protein engineering. We describe the first cellular synthesis of protein catenanes through the use of the p53 dimerization domain to guide the intertwining of two protein chains and SpyTag-SpyCatcher chemistry for efficient cyclization. The catenane topology was unambiguously proven by SDS-PAGE, SEC, and partial digestion experiments and was shown to confer enhanced stability toward trypsin digestion relative to monomeric control mutants. The assembly-reaction synergy enabled by protein folding and genetically encoded protein chemistry offers a convenient yet powerful approach for creating mechanically interlocked, complex protein topologies in vivo.

摘要

在超分子化学和蛋白质工程领域,直接通过细胞生产拓扑结构复杂的蛋白质备受关注。我们描述了蛋白质链环的首次细胞合成,该过程利用p53二聚化结构域引导两条蛋白质链相互缠绕,并借助SpyTag-SpyCatcher化学实现高效环化。通过SDS-PAGE、SEC和部分消化实验明确证实了链环拓扑结构,并且相对于单体对照突变体,该结构对胰蛋白酶消化具有更高的稳定性。蛋白质折叠和基因编码的蛋白质化学所实现的组装反应协同作用,为在体内创建机械互锁的复杂蛋白质拓扑结构提供了一种便捷而强大的方法。

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