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晶体和溶液中的MPD与DNA弯曲

MPD and DNA bending in crystals and in solution.

作者信息

Dickerson R E, Goodsell D, Kopka M L

机构信息

Department of Chemistry, University of California, Los Angeles 90095-1570, USA.

出版信息

J Mol Biol. 1996 Feb 16;256(1):108-25. doi: 10.1006/jmbi.1996.0071.

DOI:10.1006/jmbi.1996.0071
PMID:8609604
Abstract

Bending of 15 to 24 degrees is observed within crystal structures of B-DNA duplexes, is strongly sequence-dependent, and exhibits no correlation with the concentration of MPD (2-methyl-2,4-pentanediol) in the crystallizing solution. Two types of bends are observed: facultative bends or flexible hinges at junctions between regions of G.C and A.T base-pairs, and a persistent and almost obligatory bend at the center of the sequence R-G-C-Y. Only A-tracts are characteristically straight and unbent in every crystal structure examined to date. A detailed examination of normal vector plots for individual strands of a double helix provides an explanation, in terms of the stacking properties of guanine and adenine bases. The effect of high MPD concentrations, in both solution and crystal, is to decrease local bending somewhat without removing it altogether. MPD gel retardation experiments provide no basis for choosing among the three models that seek to explain macroscopic curvature of DNA by means of microscopic bending: junction being, bent A-tracts, or bent general -sequence DNA. Crystallographic data on the straightness of A-tracts, the bendability of non-A sequences, and the identity of inclination angles in A-tract and non-A-tracts B-DNA support only the general-sequence bending model. The pre-melting transition observed in A-tract DNA probably represents a relaxation of stiff adenine stacks to a flexible conformation more typical of general-sequence DNA.

摘要

在B-DNA双链体的晶体结构中观察到15至24度的弯曲,这种弯曲强烈依赖于序列,并且与结晶溶液中MPD(2-甲基-2,4-戊二醇)的浓度无关。观察到两种类型的弯曲:G.C和A.T碱基对区域之间连接处的兼性弯曲或柔性铰链,以及序列R-G-C-Y中心处持续且几乎必然的弯曲。在迄今为止检查的每个晶体结构中,只有A序列特征性地是直的且未弯曲。对双螺旋单链的法线向量图进行详细检查,根据鸟嘌呤和腺嘌呤碱基的堆积特性给出了解释。在溶液和晶体中,高浓度MPD的作用是在不完全消除局部弯曲的情况下使其有所减小。MPD凝胶阻滞实验无法在三种试图通过微观弯曲来解释DNA宏观曲率的模型中做出选择:连接处弯曲、A序列弯曲或一般序列DNA弯曲。关于A序列的直线性、非A序列的可弯曲性以及A序列和非A序列B-DNA中倾斜角一致性的晶体学数据仅支持一般序列弯曲模型。A序列DNA中观察到的预熔解转变可能代表刚性腺嘌呤堆积物松弛到一般序列DNA更典型的柔性构象。

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