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PMID: 1447218 Published · ppublish English Comparative Study Journal Article Research Support, U.S. Gov't, P.H.S.

Stereoselective interaction with chiral phosphorothioates at the central DNA kink of the EcoRI endonuclease-GAATTC complex.

The Journal of biological chemistry ·Vol. 267 ·No. 34 ·1992-12-05 ·Pages 24810-8

Lesser DR, Grajkowski A, Kurpiewski MR, Koziolkiewicz M, Stec WJ, Jen-Jacobson L

Abstract

We have probed the contacts between EcoRI endonuclease and the central phosphate of its recognition site GAApTTC, using synthetic oligonucleotides containing single stereospecific Rp- or Sp-phosphorothioates (Ps). These substitutions produce subtle stereospecific effects on EcoRI endonuclease binding and cleavage. An Sp-Ps substitution in one strand of the DNA duplex improves binding free energy by -1.5 kcal/mol, whereas the Rp-Ps substitution has an unfavorable effect (+0.3 kcal/mol) on binding free energy. These effects derive principally from changes in the first order rate constants for dissociation of the enzyme-DNA complexes. The first order rate constants for strand scission are also affected, in that a strand containing Sp-Ps substitution is cleaved 2 to 3 times more rapidly than a strand containing a normal prochiral phosphate, whereas a strand containing Rp-Ps substitution is cleaved about 3 times slower than normal. As a result, single-strand substitutions produce pronounced asymmetry in the rates of cleavage of the two DNA strands, and this effect is exaggerated in an Rp,Sp-heteroduplex. Ethylation-interference footprinting indicates that none of the Ps substitutions cause any major change in contacts between endonuclease and DNA phosphates. When an Sp-Ps localizes P = O in the DNA major groove, a hydrogen-bonding interaction with the backbone amide-NH of Gly116 of the endonuclease is improved relative to that with a prochiral phosphate having intermediate P-O bond order and delocalized charge.

MeSH Terms
Base Sequence Binding Sites DNA/chemistry,metabolism Deoxyribonuclease EcoRI/chemistry,metabolism Kinetics Models, Molecular Molecular Sequence Data Nucleic Acid Conformation Oligodeoxyribonucleotides/chemical synthesis,chemistry,metabolism Organothiophosphates/metabolism Protein Conformation Stereoisomerism Structure-Activity Relationship Substrate Specificity Thermodynamics
Chemicals
Oligodeoxyribonucleotides Organothiophosphates DNA Deoxyribonuclease EcoRI
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Lesser D R
Department of Biological Sciences, University of Pittsburgh, Pennsylvania 15260.
Grajkowski A
Kurpiewski M R
Koziolkiewicz M
Stec W J
Jen-Jacobson L
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1992-12-05
Pages
24810-8
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NIGMS NIH HHS · R01 GM029207 · United States
NIGMS NIH HHS · GM-29207 · United States
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