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小沟到大沟,由一个二脒基苯并咪唑二聚体引起的方向弯曲的不寻常的 DNA 序列依赖性变化。

Minor groove to major groove, an unusual DNA sequence-dependent change in bend directionality by a distamycin dimer.

机构信息

Department of Chemistry, Georgia State University, Atlanta, Georgia 30303, United States.

出版信息

Biochemistry. 2011 Sep 6;50(35):7674-83. doi: 10.1021/bi201010g. Epub 2011 Aug 10.

Abstract

DNA sequence-dependent conformational changes induced by the minor groove binder, distamycin, have been evaluated by polyacrylamide gel electrophoresis. The distamycin binding affinity, cooperativity, and stoichiometry with three target DNA sequences that have different sizes of alternating AT sites, ATAT, ATATA, and ATATAT, have been determined by mass spectrometry and surface plasmon resonance to help explain the conformational changes. The results show that distamycin binds strongly to and bends five or six AT base pair minor groove sites as a dimer with positive cooperativity, while it binds to ATAT as a weak, slightly anticooperative dimer. The bending direction was evaluated with an in phase A-tract reference sequence. Unlike other similar monomer minor groove binding compounds, such as netropsin, the distamycin dimer changes the directionality of the overall curvature away from the minor groove to the major groove. This distinct structural effect may allow designed distamycin derivatives to have selective therapeutic effects.

摘要

通过聚丙烯酰胺凝胶电泳评估了小沟结合物放线菌素 D 诱导的 DNA 序列依赖性构象变化。通过质谱法和表面等离子体共振测定了放线菌素 D 与三个具有不同大小交替 AT 位点的靶 DNA 序列(ATAT、ATATA 和 ATATAT)的结合亲和力、协同性和化学计量比,以帮助解释构象变化。结果表明,放线菌素 D 以二聚体的形式与 AT 碱基对小沟的五个或六个位点强烈结合,并具有正协同性,而与 ATAT 结合时则为弱的、略有反协同性二聚体。通过同相 A- 链段参考序列评估了弯曲方向。与其他类似的单体小沟结合化合物(如 netropsin)不同,放线菌素 D 二聚体改变了整体曲率的方向,使其从小沟向大沟偏离。这种独特的结构效应可能使设计的放线菌素 D 衍生物具有选择性的治疗效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d41/3164995/8f7f781ec417/nihms317968f1.jpg

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