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4′-6′-二脒基-2-苯基吲哚对DNA和多脱氧核苷酸二级结构及模板活性的影响

Influence of 4'-6'-diamidino-2-phenylindole on the secondary structure and template activities of DNA and polydeoxynucleotides.

作者信息

Chandra P, Mildner B, Dann O, Metz A

出版信息

Mol Cell Biochem. 1977 Dec 29;18(2-3):81-6. doi: 10.1007/BF00280272.

Abstract

The interaction between 4'-6-Diamidino-2-Phenylindole-hydrochloride (DAPI) and a variety of DNAs and synthetic polydeoxynucleotides was investigated in order to delineate the nucleic acid structural features necessary for binding. The spectra of DAPI-DNA complexes, measured at various DAPI:DNA molar ratios (r), are hypochromic relative to DNA in the region of its maximum absorption. All the curves pass through an isosbestic point at 268 nm. A new maxima appears in the region of 380-392 nm for DAPI-DNA COMplexes. The magnitude of the peaks in the region are directly proportional to the amount of drug present in the complex. Studies with various DNA types and synthetic polydeoxynucleotides indicate that the drug preferentially binds to dAT-rich regions of DNA. This was also confirmed by enzymatic studies. The inhibition of template action by DAPI in a purified DNA-polymerase reaction was dependent on the dAT-content of the template. The implication of these data to explain a selective binding of DAPI to mitochondrial DNA have been discussed.

摘要

研究了4′-6-二脒基-2-苯基吲哚盐酸盐(DAPI)与多种DNA及合成多脱氧核苷酸之间的相互作用,以确定结合所需的核酸结构特征。在不同的DAPI:DNA摩尔比(r)下测量的DAPI-DNA复合物光谱,在DNA最大吸收区域相对于DNA呈减色效应。所有曲线在268nm处都经过一个等吸收点。DAPI-DNA复合物在380 - 392nm区域出现一个新的最大值。该区域峰的大小与复合物中药物的含量成正比。对各种DNA类型和合成多脱氧核苷酸的研究表明,该药物优先结合于DNA中富含dAT的区域。酶学研究也证实了这一点。在纯化的DNA聚合酶反应中,DAPI对模板作用的抑制取决于模板的dAT含量。已经讨论了这些数据对解释DAPI与线粒体DNA选择性结合的意义。

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