首页> 外文期刊>Journal of molecular recognition: JMR >Probing the interaction of distamycin A with S100 beta: the 'unexpected' ability of S100 beta to bind to DNA-binding ligands
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Probing the interaction of distamycin A with S100 beta: the 'unexpected' ability of S100 beta to bind to DNA-binding ligands

机译:探究双霉素A与S100 beta的相互作用:S100 beta与DNA结合配体结合的“意外”能力

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摘要

DNA-minor-groove-binding ligands are potent antineoplastic molecules. The antibiotic distamycin A is the prototype of one class of these DNA-interfering molecules that have been largely used in vitro. The affinity of distamycin A for DNA is well known, and the structural details of the complexes with some B-DNA and G-quadruplex-forming DNA sequences have been already elucidated. Here, we show that distamycin A binds S100, a protein involved in the regulation of several cellular processes. The reported affinity of distamycin A for the calcium(II)-loaded S100 reinforces the idea that some biological activities of the DNA-minor-groove-binding ligands arise from the binding to cellular proteins. Copyright (c) 2015 John Wiley & Sons, Ltd.
机译:DNA小沟结合配体是有效的抗肿瘤分子。抗生素双歧霉素A是这类已广泛用于体外的DNA干扰分子的原型。双斯坦霉素A对DNA的亲和力是众所周知的,并且已经阐明了与一些B-DNA和形成G-四链体的DNA序列的复合物的结构细节。在这里,我们显示了双霉素A结合S100,S100是一种参与多种细胞过程调控的蛋白质。已报道的间他霉素A对负载钙(II)的S100的亲和力加强了这样一种观念,即DNA小沟结合配体的某些生物学活性源自与细胞蛋白的结合。版权所有(c)2015 John Wiley&Sons,Ltd.

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