Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
34
|
pubmed:dateCreated |
1992-12-30
|
pubmed:abstractText |
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.
|
pubmed:grant | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Dec
|
pubmed:issn |
0021-9258
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
5
|
pubmed:volume |
267
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
24810-8
|
pubmed:dateRevised |
2007-11-14
|
pubmed:meshHeading |
pubmed-meshheading:1447218-Base Sequence,
pubmed-meshheading:1447218-Binding Sites,
pubmed-meshheading:1447218-DNA,
pubmed-meshheading:1447218-Deoxyribonuclease EcoRI,
pubmed-meshheading:1447218-Kinetics,
pubmed-meshheading:1447218-Models, Molecular,
pubmed-meshheading:1447218-Molecular Sequence Data,
pubmed-meshheading:1447218-Nucleic Acid Conformation,
pubmed-meshheading:1447218-Oligodeoxyribonucleotides,
pubmed-meshheading:1447218-Protein Conformation,
pubmed-meshheading:1447218-Stereoisomerism,
pubmed-meshheading:1447218-Structure-Activity Relationship,
pubmed-meshheading:1447218-Substrate Specificity,
pubmed-meshheading:1447218-Thermodynamics,
pubmed-meshheading:1447218-Thiophosphoric Acid Esters
|
pubmed:year |
1992
|
pubmed:articleTitle |
Stereoselective interaction with chiral phosphorothioates at the central DNA kink of the EcoRI endonuclease-GAATTC complex.
|
pubmed:affiliation |
Department of Biological Sciences, University of Pittsburgh, Pennsylvania 15260.
|
pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, U.S. Gov't, P.H.S.
|