Specific interactions of distamycin with G-quadruplex DNA

被引:83
作者
Cocco, MJ [1 ]
Hanakahi, LA
Huber, MD
Maizels, N
机构
[1] Yale Univ, Dept Mol Biophys & Biochem, New Haven, CT 06520 USA
[2] Johns Hopkins Univ, Dept Biochem & Mol Biol, Bloomberg Sch Publ Hlth, Baltimore, MD 21205 USA
[3] Univ Washington, Sch Med, Dept Immunol, Seattle, WA 98195 USA
[4] Univ Washington, Sch Med, Dept Biochem, Seattle, WA 98195 USA
关键词
D O I
10.1093/nar/gkg392
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:2944 / 2951
页数:8
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