Protein Science by DNA Sequencing: How Advances in Molecular Biology Are Accelerating Biochemistry

被引:9
|
作者
Higgins, Sean A. [1 ]
Savage, David F. [1 ,2 ]
机构
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, 229 Stanley Hall, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
基金
美国国家卫生研究院;
关键词
RANDOM CIRCULAR PERMUTATION; TEM-1; BETA-LACTAMASE; AMINO-ACID DELETION; DIRECTED EVOLUTION; IN-VIVO; TARGETED MUTAGENESIS; FITNESS LANDSCAPES; ENZYME; BINDING; GENES;
D O I
10.1021/acs.biochem.7b00886
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A fundamental goal of protein biochemistry is to determine the sequence-function relationship, but the vastness of sequence space makes comprehensive evaluation of this landscape difficult. However, advances in DNA synthesis and sequencing now allow researchers to assess the functional impact of every single mutation in many proteins, but challenges remain in library construction and the development of general assays applicable to a diverse range of protein functions. This Perspective briefly outlines the technical innovations in DNA manipulation that allow massively parallel protein biochemistry and then summarizes the methods currently available for library construction and the functional assays of protein variants. Areas in need of future innovation are highlighted with a particular focus on assay development and the use of computational analysis with machine learning to effectively traverse the sequence-function landscape. Finally, applications in the fundamentals of protein biochemistry, disease prediction, and protein engineering are presented.
引用
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页码:38 / 46
页数:9
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