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通过DNA结合基序SPKK对DNA进行结构修饰:利用紫外共振拉曼光谱检测碱基对氢键和碱基堆积的变化

Structural modification of DNA by a DNA-binding motif SPKK: detection of changes in base-pair hydrogen bonding and base stacking by UV resonance Raman spectroscopy.

作者信息

Takeuchi H, Sasamori J

机构信息

Pharmaceutical Institute, Tohoku University, Japan.

出版信息

Biopolymers. 1995 Apr;35(4):359-67. doi: 10.1002/bip.360350403.

Abstract

Interactions of a DNA-binding motif SPKK with polynucleotides have been investigated by uv resonance Raman spectroscopy. Analysis of the Raman spectra has shown that the tetrapeptide SPKK weakens the adenine-thymine base-pair hydrogen bonding in poly(dA-dT).poly(dA-dT) and reduces the adenine-adenine base stacking interactions in poly(dA).poly(dT), both effects being indicative of destabilization of the DNA double helical structure. On the other hand, poly(dG-dC).poly(dG-dC) and poly(dG).poly(dC) do not show any structural change in the presence of SPKK. The present observations confirm that the SPKK motif, which is frequently found in histone H1 proteins, specifically binds to A/T-rich regions of DNA and loosens the DNA double-helical structure. One of the roles of the SPKK motifs in histones may be to increase DNA flexibility so that DNA can wrap around core histones and be assembled into chromosomes more easily.

摘要

通过紫外共振拉曼光谱研究了DNA结合基序SPKK与多核苷酸的相互作用。拉曼光谱分析表明,四肽SPKK削弱了聚(dA-dT)·聚(dA-dT)中腺嘌呤-胸腺嘧啶碱基对的氢键,并减少了聚(dA)·聚(dT)中腺嘌呤-腺嘌呤碱基堆积相互作用,这两种效应均表明DNA双螺旋结构不稳定。另一方面,在SPKK存在的情况下,聚(dG-dC)·聚(dG-dC)和聚(dG)·聚(dC)未显示任何结构变化。目前的观察结果证实,在组蛋白H1中经常发现的SPKK基序特异性结合富含A/T的DNA区域,并使DNA双螺旋结构松弛。组蛋白中SPKK基序的作用之一可能是增加DNA的柔韧性,以便DNA能够缠绕在核心组蛋白周围并更容易组装成染色体。

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