Isolation and crystallization of a chimeric Qβ replicase containing Thermus thermophilus EF-Ts

Qβ replicase is a protein complex responsible for the replication of the genomic RNA of bacteriophage Qβ. In addition to the phage-encoded catalytic β subunit, it recruits three proteins from the host Escherichia coli cell: elongation factors EF-Tu and EF-Ts and ribosomal protein S1. We prepared a c...

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Veröffentlicht in:Biochemistry (Moscow) 2010-08, Vol.75 (8), p.989-994
Hauptverfasser: Vasiliev, N. N, Jenner, L, Yusupov, M. M, Chetverin, A. B
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Sprache:eng
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Zusammenfassung:Qβ replicase is a protein complex responsible for the replication of the genomic RNA of bacteriophage Qβ. In addition to the phage-encoded catalytic β subunit, it recruits three proteins from the host Escherichia coli cell: elongation factors EF-Tu and EF-Ts and ribosomal protein S1. We prepared a chimeric Qβ replicase in which the E. coli EF-Ts is replaced with EF-Ts from Thermus thermophilus. The chimeric protein is produced in E. coli cells during coexpression of the genes encoding the β subunit and thermophilic EF-Ts. The developed isolation procedure yields a substantially homogeneous preparation of the chimeric replicase. Unlike the wild-type enzyme, the S1-less chimeric replicase could be crystallized. This result facilitates studies on the structure of Qβ replicase and the mechanism of recognition of its templates that can replicate in vitro at a record rate.
ISSN:0006-2979
1608-3040
1608-3040
DOI:10.1134/S0006297910080067