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通过单克隆自身免疫抗体结合检测到的双链DNA构象变化

Variations in duplex DNA conformation detected by the binding of monoclonal autoimmune antibodies.

作者信息

Braun R P, Lee J S

出版信息

Nucleic Acids Res. 1986 Jun 25;14(12):5049-65. doi: 10.1093/nar/14.12.5049.

Abstract

Four monoclonal antibodies (Jel 229, 239, 241, 242) which bound to duplex DNA were prepared from two autoimmune female NZB/NZW mice. Their binding to various nucleic acids was investigated by a competitive solid phase radioimmune assay which allows the estimation of relative binding constants. None of the antibodies showed any consistent variation of binding constant with base composition and thus they must recognize features of the DNA backbone. Jel 241 binds across the major groove but the interaction with poly(pyrimidine) X poly(purine) DNAs was barely detectable. This antibody appears to recognize the "alternating-B" conformation which is promoted by methylation of pyrimidines in alternating sequences. The other three antibodies bind in the minor groove. In particular, for Jel 229 the preferred antigen was poly(dG) X poly(dC) with only weak binding to poly(dA) X poly(dT). This suggests a requirement for a wide minor groove. Thus autoimmune antibodies provide examples of "analogue" recognition and can be used to detect structural variations in the grooves of duplex DNA.

摘要

从两只自身免疫的雌性新西兰黑/新西兰白(NZB/NZW)小鼠中制备了四种与双链DNA结合的单克隆抗体(Jel 229、239、241、242)。通过竞争性固相放射免疫测定法研究了它们与各种核酸的结合情况,该方法可用于估计相对结合常数。这些抗体均未表现出结合常数随碱基组成的任何一致变化,因此它们必定识别的是DNA骨架的特征。Jel 241跨大沟结合,但与聚(嘧啶)×聚(嘌呤)DNA的相互作用几乎检测不到。该抗体似乎识别由交替序列中嘧啶甲基化所促进的“交替B”构象。其他三种抗体在小沟中结合。特别是,对于Jel 229而言,其优选抗原是聚(dG)×聚(dC),而与聚(dA)×聚(dT)的结合较弱。这表明需要较宽的小沟。因此,自身免疫抗体提供了“类似物”识别的实例,可用于检测双链DNA沟中的结构变化。

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