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PMID: 7937087 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Mutations that increase the affinity of a translational repressor for RNA.

Nucleic acids research ·Vol. 22 ·No. 18 ·1994-09-11 ·Pages 3748-52

Lim F, Peabody DS

Abstract

The coat protein of the RNA bacteriophage MS2 is a specific RNA binding protein that represses translation of the viral replicase gene during the infection cycle. As an approach to characterizing the RNA-binding site of coat protein we have isolated a series of coat mutants that suppress the effects of a mutation in the translational operator. Each of the mutants exhibits a super-repressor phenotype, more tightly repressing both the mutant and wild-type operators than does the wild-type protein. The variant coat proteins were purified and subjected to filter binding assays to determine their affinities for the mutant and wild-type operators. Each protein binds the operators from 3 to 7.5-fold more tightly than normal coat protein. The amino acid substitutions seem to extend the normal binding site by introducing new interactions with RNA.

MeSH Terms
Base Sequence Capsid/chemistry,genetics,metabolism Kinetics Levivirus/metabolism Models, Molecular Molecular Sequence Data Mutation/physiology Nucleic Acid Conformation Protein Biosynthesis RNA, Viral/chemistry,metabolism RNA-Binding Proteins/chemistry,genetics,metabolism RNA-Dependent RNA Polymerase/genetics Suppression, Genetic
Chemicals
RNA, Viral RNA-Binding Proteins RNA-Dependent RNA Polymerase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Lim F
Department of Cell Biology, University of New Mexico School of Medicine, Albuquerque 87131.
Peabody D S
References (11)
11 references, click to expand
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Article Info
Journal
Nucleic acids research
Abbr.
Nucleic Acids Res
ISSN
0305-1048
Published
1994-09-11
Pages
3748-52
Language
English
Region
England
NLM ID
0411011
PMCID
PMC308357
Subset
IM
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