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PMID: 6347247 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Sequence-specific interaction of R17 coat protein with its ribonucleic acid binding site.

Biochemistry ·Vol. 22 ·No. 11 ·1983-05-24 ·Pages 2601-10

Carey J, Cameron V, de Haseth PL, Uhlenbeck OC

Abstract

The interaction between phage R17 coat protein and its RNA binding site for translational repression was studied as an example of a sequence-specific RNA--protein interaction. Nuclease protection and selection experiments define the binding site to about 20 contiguous nucleotides which form a hairpin. A nitrocellulose filter retention assay is used to show that the binding between the coat protein and a synthetic 21-nucleotide RNA fragment conforms to a simple bimolecular reaction. Unit stoichiometry and a Kd of about 1 nM are obtained at 2 degrees C in buffer containing 0.19 M salt. The interaction is highly sequence specific since a variety of RNAs failed to compete with the 21-nucleotide fragment for coat protein binding.

MeSH Terms
Amino Acid Sequence Base Sequence Binding, Competitive Capsid/metabolism Capsid Proteins Coliphages/metabolism Escherichia coli/metabolism Nucleic Acid Conformation RNA, Viral/metabolism RNA-Binding Proteins Viral Proteins/isolation & purification,metabolism
Chemicals
Capsid Proteins RNA, Viral RNA-Binding Proteins Viral Proteins
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Carey J
Cameron V
de Haseth P L
Uhlenbeck O C
Article Info
Journal
Biochemistry
Abbr.
Biochemistry
ISSN
0006-2960
Published
1983-05-24
Pages
2601-10
Language
English
Region
United States
NLM ID
0370623
Subset
IM
Grants
NIGMS NIH HHS · GM 19059 · United States
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