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双链DNA对S1核酸酶敏感性的结构基础。

A structural basis for S1 nuclease sensitivity of double-stranded DNA.

作者信息

Pulleyblank D E, Haniford D B, Morgan A R

出版信息

Cell. 1985 Aug;42(1):271-80. doi: 10.1016/s0092-8674(85)80122-7.

Abstract

A protonated form of a cloned simple repeating DNA sequence d(TC)n X d(GA) is detectable in equilibrium with the usual Watson-Crick base-paired form at pHs up to 7. This form is anomalously sensitive to a variety of single-strand-specific endonucleases. The observed pH dependent protection of N-7 of dG residues within the insert suggests that these residues are either Hoogsteen or reverse Hoogsteen base-paired to protonated dC residues of the polypyrimidine strand. A structure in which dA:dT Watson-Crick base pairs alternate with Hoogsteen syndG:dCH+ pairs appears to be the most stereochemically acceptable structure consistent with the chemical properties of this protonated DNA. Protonated d(TC)n X d(GA)n interacts with an anti-Z DNA antibody raised against brominated d(GC)n X d(GC)n.

摘要

在pH值高达7时,克隆的简单重复DNA序列d(TC)n X d(GA)的质子化形式可与常见的沃森-克里克碱基配对形式达到平衡并被检测到。这种形式对多种单链特异性核酸内切酶异常敏感。观察到的插入片段内dG残基N-7的pH依赖性保护表明,这些残基要么以Hoogsteen配对,要么以反向Hoogsteen配对与多嘧啶链的质子化dC残基结合。一种dA:dT沃森-克里克碱基对与Hoogsteen型dG:dCH+对交替出现的结构似乎是与这种质子化DNA化学性质相符的最符合立体化学要求的结构。质子化的d(TC)n X d(GA)n与针对溴化d(GC)n X d(GC)n产生的抗Z-DNA抗体相互作用。

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