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PMID: 3120311 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Synthesis of a sequence-specific DNA-cleaving peptide.

Science (New York, N.Y.) ·Vol. 238 ·No. 4830 ·1987-11-20 ·Pages 1129-32

Sluka JP, Horvath SJ, Bruist MF, Simon MI, Dervan PB

Abstract

A synthetic 52-residue peptide based on the sequence-specific DNA-binding domain of Hin recombinase (139-190) has been equipped with ethylenediaminetetraacetic acid (EDTA) at the amino terminus. In the presence of Fe(II), this synthetic EDTA-peptide cleaves DNA at Hin recombination sites. The cleavage data reveal that the amino terminus of Hin(139-190) is bound in the minor groove of DNA near the symmetry axis of Hin recombination sites. This work demonstrates the construction of a hybrid peptide combining two functional domains: sequence-specific DNA binding and DNA cleavage.

MeSH Terms
Bacterial Proteins/metabolism DNA/metabolism DNA Nucleotidyltransferases/metabolism DNA-Binding Proteins/chemical synthesis Edetic Acid Ferrous Compounds Models, Molecular Nucleic Acid Conformation Oxidation-Reduction Peptide Fragments Protein Binding Structure-Activity Relationship
Chemicals
Bacterial Proteins DNA-Binding Proteins Ferrous Compounds Peptide Fragments DNA Edetic Acid DNA Nucleotidyltransferases Hin recombinase
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Sluka J P
Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena 91125.
Horvath S J
Bruist M F
Simon M I
Dervan P B
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1987-11-20
Pages
1129-32
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NIGMS NIH HHS · GM-09534-02 · United States
NIGMS NIH HHS · T32GM07616 · United States
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