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首页> 外文期刊>Biochemistry >Minor Groove to Major Groove, an Unusual DNA Sequence-Dependent Change in Bend Directionality by a Distamycin Dimer
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Minor Groove to Major Groove, an Unusual DNA Sequence-Dependent Change in Bend Directionality by a Distamycin Dimer

机译:小沟槽到大沟槽,由Distamycin Dimer弯曲方向的异常DNA序列依赖性变化

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摘要

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.
机译:通过聚丙烯酰胺凝胶电泳已评估了由小沟结合剂双霉素引起的DNA序列依赖性构象变化。通过质谱和表面等离振子共振已经确定了与具有不同大小的交替AT位点的三个目标DNA序列(ATAT,ATATA和ATATAT)的二霉素结合亲和力,协同作用和化学计量关系,以帮助解释构象变化。结果显示,他霉素与五或六个AT碱基对小沟位点牢固结合并弯曲,形成具有正协同性的二聚体,而与ATAT结合时则为弱的,稍微反协同的二聚体。使用同相A方向参考序列评估弯曲方向。与其他类似的单体小沟结合化合物(如netropsin)不同,二霉素二聚体可将总曲率的方向从小沟改为大沟。这种独特的结构作用可以使设计的二他霉素衍生物具有选择性的治疗作用。

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