Specific interactions of distamycin with G-quadruplex DNA
AUTOR(ES)
Cocco, Melanie J.
FONTE
Oxford University Press
RESUMO
Distamycin binds the minor groove of duplex DNA at AT-rich regions and has been a valuable probe of protein interactions with double-stranded DNA. We find that distamycin can also inhibit protein interactions with G-quadruplex (G4) DNA, a stable four-stranded structure in which the repeating unit is a G-quartet. Using NMR, we show that distamycin binds specifically to G4 DNA, stacking on the terminal G-quartets and contacting the flanking bases. These results demonstrate the utility of distamycin as a probe of G4 DNA–protein interactions and show that there are (at least) two distinct modes of protein–G4 DNA recognition which can be distinguished by sensitivity to distamycin.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=156726Documentos Relacionados
- Cell senescence and telomere shortening induced by a new series of specific G-quadruplex DNA ligands
- A G-quadruplex Stabilizer Induces M-phase Cell Cycle Arrest*
- Small-Molecule Selectively Recognizes Human Telomeric G-Quadruplex DNA and Regulates Its Conformational Switch
- Phosphorylation at 5′ end of guanosine stretches inhibits dimerization of G-quadruplexes and formation of a G-quadruplex interferes with the enzymatic activities of DNA enzymes
- Structural transition from antiparallel to parallel G-quadruplex of d(G4T4G4) induced by Ca2+