Theoretical study of the guanine --> 6-thioguanine substitution in duplexes, triplexes, and tetraplexes
Jazyk angličtina Země Spojené státy americké Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
15521784
DOI
10.1021/ja0468628
Knihovny.cz E-zdroje
- MeSH
- DNA chemie MeSH
- guanin chemie MeSH
- konformace nukleové kyseliny MeSH
- molekulární modely MeSH
- termodynamika MeSH
- thioguanin chemie MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- DNA MeSH
- guanin MeSH
- thioguanin MeSH
- triplex DNA MeSH Prohlížeč
Molecular dynamics and thermodynamic integration calculations have been carried out on a set of G-rich single-strand, duplex, triplex, and quadruplex DNAs to study the structural and stability changes connected with the guanine --> 6-thioguanine (G --> S) mutation. The presence of 6-thioguanine leads to a shift of the geometry from the B/A intermediate to the pure B-form in duplex DNA. The G --> S mutation does not largely affect the structure of the antiparallel triplex when it is located at the reverse-Hoogsteen position, but leads to a non-negligible local distortion in the structure when it is located at the Watson-Crick position. The G --> S mutation leads to destabilization of all studied structures: the lowest effect has been observed for the G --> S mutation in the reverse-Hoogsteen strand of the triplex, a medium effect has been observed in the Watson-Crick strand of the triplex and duplex, and the highest influence of the G -->S mutation has been found for the quadruplex structures.
Citace poskytuje Crossref.org
Molecular dynamics simulations and their application to four-stranded DNA