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特定的小沟溶剂化作用是DNA结合位点识别的关键决定因素。

Specific minor groove solvation is a crucial determinant of DNA binding site recognition.

作者信息

Harris Lydia-Ann, Williams Loren Dean, Koudelka Gerald B

机构信息

Department of Biological Sciences, 607 Cooke Hall, University at Buffalo, Buffalo, NY 14260, USA.

School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, GA 30332-0400, USA.

出版信息

Nucleic Acids Res. 2014 Dec 16;42(22):14053-9. doi: 10.1093/nar/gku1259. Epub 2014 Nov 27.

Abstract

The DNA sequence preferences of nearly all sequence specific DNA binding proteins are influenced by the identities of bases that are not directly contacted by protein. Discrimination between non-contacted base sequences is commonly based on the differential abilities of DNA sequences to allow narrowing of the DNA minor groove. However, the factors that govern the propensity of minor groove narrowing are not completely understood. Here we show that the differential abilities of various DNA sequences to support formation of a highly ordered and stable minor groove solvation network are a key determinant of non-contacted base recognition by a sequence-specific binding protein. In addition, disrupting the solvent network in the non-contacted region of the binding site alters the protein's ability to recognize contacted base sequences at positions 5-6 bases away. This observation suggests that DNA solvent interactions link contacted and non-contacted base recognition by the protein.

摘要

几乎所有序列特异性DNA结合蛋白的DNA序列偏好都受到未与蛋白质直接接触的碱基的影响。对未接触碱基序列的区分通常基于DNA序列使DNA小沟变窄的不同能力。然而,控制小沟变窄倾向的因素尚未完全了解。在这里,我们表明,各种DNA序列支持形成高度有序且稳定的小沟溶剂化网络的不同能力,是序列特异性结合蛋白对未接触碱基识别的关键决定因素。此外,破坏结合位点未接触区域的溶剂网络会改变蛋白质识别相距5至6个碱基位置处接触碱基序列的能力。这一观察结果表明,DNA与溶剂的相互作用将蛋白质对接触碱基和未接触碱基的识别联系起来。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b767/4267663/40e1eaabc8dc/gku1259fig1.jpg

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