热稳定性
多序列比对
序列(生物学)
蛋白质工程
计算生物学
序列比对
自由序列分析
序列空间
生物
结构线形
共识序列
序列分析
蛋白质设计
蛋白质测序
功能(生物学)
定向进化
遗传学
肽序列
蛋白质结构
生物信息学
基因
突变体
生物化学
酶
数学
巴拿赫空间
纯数学
作者
Tianwen Wang,Chen Liang,Yajing Hou,Mengyuan Zheng,Hongju Xu,Yafei An,Sa Xiao,Lu Liu,Shuaibin Lian
标识
DOI:10.1007/s10529-020-02914-0
摘要
Multiple sequence alignment (MSA) is a fundamental way to gain information that cannot be obtained from the analysis of any individual sequence included in the alignment. It provides ways to investigate the relationship between sequence and function from a perspective of evolution. Thus, the MSA of proteins can be employed as a reference for protein engineering. In this paper, we reviewed the recent advances to highlight how protein engineering was benefited from the MSA of proteins. These methods include (1) engineering the thermostability or solubility of proteins by making it closer to the consensus sequence of the alignment through introducing site mutations; (2) structure-based engineering proteins with comparative modeling; (3) creating paleoenzymes featured with high thermostability and promiscuity by constructing the ancestral sequences derived from multiple sequence alignment; and (4) incorporating site-mutations targeting the evolutionarily coupled sites identified from multiple sequence alignment.
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