DRUG-BINDING BY BRANCHED DNA - SELECTIVE INTERACTION OF THE DYE STAINS-ALL WITH AN IMMOBILE JUNCTION

被引:25
作者
LU, M [1 ]
GUO, Q [1 ]
SEEMAN, NC [1 ]
KALLENBACH, NR [1 ]
机构
[1] NYU,DEPT CHEM,NEW YORK,NY 10003
关键词
D O I
10.1021/bi00465a038
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
The thiacarbocyanine dye Stains-All (4,5:4′,5′-dibenzo-3,3′-diethyl-9-methylthiacarbocyanine bromide) is one of a large number of cyanine dyes introduced as photosensitizers in the photographic industry. Stains-All is used in histology as a stain for nucleic acids, proteins, polysaccharides, and lipids. We report here that the dye colors branched DNA molecules differently from linear duplexes and use footprinting experiments with methidiumpropyl-EDTA•Fe(II) [MPE•Fe(II)] and bis(o-phenanthroline)copper(I) [(O-P)2Cu(I)] to show that Stains-All interacts preferentially at the branch point of a four-arm DNA structure. A titration experiment allows us to estimate that the interaction of the dye with the branch has a dissociation constant below 45 nM, tighter than that of ethidium or methidium by over 2 orders of magnitude. Probing the interaction with the purine-specific reagent diethyl pyrocarbonate (DEPC) implies that the dye induces an asymmetric distortion near the branch in the major grooves of double helix in the junction. © 1990, American Chemical Society. All rights reserved.
引用
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页码:3407 / 3412
页数:6
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