Directed polymerase evolution

被引:48
作者
Chen, Tingjian [1 ]
Romesberg, Floyd E. [1 ]
机构
[1] Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA
基金
美国国家卫生研究院;
关键词
Directed evolution; Polymerase; Modified nucleotide; Protein engineering; AQUATICUS DNA-POLYMERASE; I KLENOW FRAGMENT; REVERSE-TRANSCRIPTASE ACTIVITY; EXPANDED GENETIC ALPHABET; UNNATURAL BASE-PAIR; RNA-POLYMERASE; KINETIC MECHANISM; MISMATCH-EXTENSION; PROTEIN EVOLUTION; ESCHERICHIA-COLI;
D O I
10.1016/j.febslet.2013.10.040
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
Polymerases evolved in nature to synthesize DNA and RNA, and they underlie the storage and flow of genetic information in all cells. The availability of these enzymes for use at the bench has driven a revolution in biotechnology and medicinal research; however, polymerases did not evolve to function efficiently under the conditions required for some applications and their high substrate fidelity precludes their use for most applications that involve modified substrates. To circumvent these limitations, researchers have turned to directed evolution to tailor the properties and/or substrate repertoire of polymerases for different applications, and several systems have been developed for this purpose. These systems draw on different methods of creating a pool of randomly mutated polymerases and are differentiated by the process used to isolate the most fit members. A variety of polymerases have been evolved, providing new or improved functionality, as well as interesting new insight into the factors governing activity. (C) 2013 Federation of European Biochemical Societies. Published by Elsevier B. V. All rights reserved.
引用
收藏
页码:219 / 229
页数:11
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