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配体结合时的DNA弯曲;DNA持久长度的变化。

DNA-bending on ligand binding; change of DNA persistence length.

作者信息

Schütz H, Reinert K E

机构信息

Institute of Microbiology and Experimental Therapy, Department of Biophysical Chemistry, Jena, Germany.

出版信息

J Biomol Struct Dyn. 1991 Oct;9(2):315-29. doi: 10.1080/07391102.1991.10507915.

Abstract

This paper simulates the helix-characteristic changes of apparent DNA persistence length caused by randomly distributed helix bends as induced, e.g., by DNA-bound ligand molecules. The parameters varied are the constant angle gamma of helix bending and the size alpha of the DNA drug binding site, but also the degree of DNA-ligand binding cooperativity and the helix-unwinding angle. If the size of the binding site is comparable with the helix pitch, the influence of phasing between helix bends and helix screw upon the apparent persistence length is obvious. In the accompanying paper experimental data are analyzed in terms of this theoretical background.

摘要

本文模拟了由随机分布的螺旋弯曲(例如由与DNA结合的配体分子诱导产生)所导致的表观DNA持久长度的螺旋特征变化。变化的参数包括螺旋弯曲的恒定角度γ、DNA药物结合位点的大小α,还有DNA-配体结合协同性程度以及螺旋解旋角度。如果结合位点的大小与螺旋螺距相当,那么螺旋弯曲与螺旋螺旋之间的相位对表观持久长度的影响就很明显。在随附论文中,将根据这一理论背景对实验数据进行分析。

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