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通过嫁接和稳定化进行计算蛋白质设计

Computational Protein Design Through Grafting and Stabilization.

作者信息

Zhu Cheng, Mowrey David D, Dokholyan Nikolay V

机构信息

Department of Biochemistry and Biophysics, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599, USA.

出版信息

Methods Mol Biol. 2017;1529:227-241. doi: 10.1007/978-1-4939-6637-0_11.

Abstract

Computational grafting of target residues onto existing protein scaffolds is a powerful method for the design of proteins with novel function. In the grafting method side chain mutations are introduced into a preexisting protein scaffold to recreate a target functional motif. The success of this approach relies on two primary criteria: (1) the availability of compatible structural scaffolds, and (2) the introduction of mutations that do not affect the protein structure or stability. To identify compatible structural motifs we use the Erebus webserver, to search the protein data bank (PDB) for user-defined structural scaffolds. To identify potential design mutations we use the Eris webserver, which accurately predicts changes in protein stability resulting from mutations. Mutations that increase the protein stability are more likely to maintain the protein structure and therefore produce the desired function. Together these tools provide effective methods for identifying existing templates and guiding further design experiments. The software tools for scaffold searching and design are available at http://dokhlab.org .

摘要

将目标残基计算性嫁接到现有蛋白质支架上是设计具有新功能蛋白质的一种强大方法。在嫁接方法中,侧链突变被引入到预先存在的蛋白质支架中以重现目标功能基序。这种方法的成功依赖于两个主要标准:(1)兼容结构支架的可用性,以及(2)引入不影响蛋白质结构或稳定性的突变。为了识别兼容的结构基序,我们使用Erebus网络服务器,在蛋白质数据库(PDB)中搜索用户定义的结构支架。为了识别潜在的设计突变,我们使用Eris网络服务器,它能准确预测突变导致的蛋白质稳定性变化。增加蛋白质稳定性的突变更有可能维持蛋白质结构,从而产生所需的功能。这些工具共同提供了识别现有模板和指导进一步设计实验的有效方法。用于支架搜索和设计的软件工具可在http://dokhlab.org获得。

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