Directed Evolution of an Error-Prone T7 DNA Polymerase that Attenuates Viral Replication

被引:7
|
作者
Soete, Sandra [2 ]
Kleine, Stefan [1 ]
Schlicke, Marina [3 ]
Brakmann, Susanne [1 ]
机构
[1] Tech Univ Dortmund, Fac Chem, Dept Chem Biol BCMT, D-44227 Dortmund, Germany
[2] Univ Cologne, Inst Biochem 2, D-50931 Cologne, Germany
[3] Univ Hosp Children & Adolescents, D-04103 Leipzig, Germany
关键词
directed evolution; DNA polymerase; DNA replication; phage; viruses; ESCHERICHIA-COLI THIOREDOXIN; RNA-POLYMERASE; VIRUS; BACTERIOPHAGE-T7; CATASTROPHE; MUTAGENESIS; MUTATION; PROCESSIVITY; FIDELITY; MUTANT;
D O I
10.1002/cbic.201000799
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
Experimental evidence exists that RNA viruses replicate with extremely high mutation rates that result in significant genetic diversity. The diverse nature of viral populations allows rapid adaptation to dynamic environments, and evolution of resistances to vaccines as well as antiviral substances. For DNA viruses that replicate at much greater fidelities, as yet, neither diverse structures in the population nor their responses to increased mutation rates have been sufficiently described. By using the example of DNA bacteriophage T7, we describe the identification of virus-specific DNA polymerase variants with decreased replication fidelities, and their impact on the efficiency of the viral infection cycle.
引用
收藏
页码:1551 / 1558
页数:8
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