首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Exposure of DNA bases induced by the interaction of DNA and calf thymus DNA helix-destabilizing protein.
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Exposure of DNA bases induced by the interaction of DNA and calf thymus DNA helix-destabilizing protein.

机译:DNA和小牛胸腺DNA螺旋不稳定蛋白的相互作用诱导的DNA碱基暴露。

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摘要

The reaction of chloroacetaldehyde with adenine bases in DNA to give a fluorescent product was used to study the availability to intermolecular reaction of positions 1 and 6 of adenine in DNA complexes with calf thymus DNA helix-destabilizing protein. No inhibition of this reaction was observed when heat-denatured DNA was complexed with the protein at a protein/DNA weight ratio of 10:1, compared to free DNA. On the contrary, the same reaction was inhibited markedly for denatured DNA in the presence of calf thymus histone HI at protein/DNA weight ratio of 2:1. Furthermore, the exchange rate for hydrogens of amino and imide groups of DNA bases in DNA strands with deuterium in the solvent was totally unaffected upon complexing of DNA with the DNA helix-destabilizing protein as examined by stopped-flow ultraviolet spectroscopy. These results indicate that the DNA helix-destabilizing protein forms a complex with single-stranded DNA, leaving DNA bases uncovered by the protein. The fluorescence intensity of DNA pretreated with chloroacetaldehyde was amplified by nearly 3-fold upon addition of the DNA helix-destabilizing protein. The possibility of "unstacking" of DNA bases induced by the protein is discussed.
机译:氯乙醛与DNA中的腺嘌呤碱基的反应生成荧光产物,用于研究小牛胸腺DNA螺旋不稳定蛋白与DNA配合物中腺嘌呤1位和6位分子间反应的有效性。当热变性的DNA与蛋白质以10:1的蛋白质/ DNA重量比与游离DNA相比复合时,未观察到对该反应的抑制。相反,在小牛胸腺组蛋白HI存在下,蛋白质/ DNA重量比为2:1时,变性DNA显着抑制了相同的反应。此外,如通过停止流紫外光谱法检查的那样,当DNA与DNA螺旋失稳蛋白复合时,DNA链中的DNA链中的氨基酸碱基的氨基和酰亚胺基的氢与溶剂中的氢的交换速率完全不受影响。这些结果表明,DNA螺旋不稳定蛋白与单链DNA形成复合物,而DNA碱基未被该蛋白覆盖。加入DNA螺旋不稳定蛋白后,用氯乙醛预处理的DNA的荧光强度增加了近3倍。讨论了由蛋白质诱导的DNA碱基“解叠”的可能性。

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