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本文引用的文献

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Probing the role of hydrogen bonds in the stability of base pairs in double-helical DNA.探究氢键在双螺旋DNA碱基对稳定性中的作用。
Biopolymers. 2007;87(2-3):165-73. doi: 10.1002/bip.20811.
2
Sequence-dependence of the energetics of opening of at basepairs in DNA.DNA中碱基对打开能量学的序列依赖性。
Biophys J. 2004 Oct;87(4):2545-51. doi: 10.1529/biophysj.104.045179.
3
Probing site-specific energetics in proteins and nucleic acids by hydrogen exchange and nuclear magnetic resonance spectroscopy.通过氢交换和核磁共振光谱探究蛋白质和核酸中特定位点的能量学。
Methods Enzymol. 2004;379:152-75. doi: 10.1016/S0076-6879(04)79009-6.
4
Cations as hydrogen bond donors: a view of electrostatic interactions in DNA.作为氢键供体的阳离子:DNA中静电相互作用的一种观点
Annu Rev Biophys Biomol Struct. 2003;32:27-45. doi: 10.1146/annurev.biophys.32.110601.141726. Epub 2003 Feb 14.
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Structural and catalytic roles for divalent magnesium in nucleic acid biochemistry.二价镁离子在核酸生物化学中的结构与催化作用
Biometals. 2002 Sep;15(3):211-23. doi: 10.1023/a:1016070614042.
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DNA-cation interactions: quo vadis?DNA与阳离子的相互作用:何去何从?
Chem Biol. 2002 Mar;9(3):277-86. doi: 10.1016/s1074-5521(02)00116-3.
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DNA-cation interactions: The major and minor grooves are flexible ionophores.
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A signature of the T ---> R transition in human hemoglobin.人类血红蛋白中T(紧张态)向R(松弛态)转变的一个特征。
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9
1 A crystal structures of B-DNA reveal sequence-specific binding and groove-specific bending of DNA by magnesium and calcium.1 B-DNA的晶体结构揭示了镁和钙对DNA的序列特异性结合和沟特异性弯曲。
J Mol Biol. 2000 Aug 25;301(4):915-45. doi: 10.1006/jmbi.2000.4012.
10
Base-catalysis of imino proton exchange in DNA: effects of catalyst upon DNA structure and dynamics.DNA中亚氨基质子交换的碱催化作用:催化剂对DNA结构和动力学的影响。
Biochemistry. 1996 Jun 25;35(25):8439-49. doi: 10.1021/bi952932z.

镁离子对DNA碱基对自发打开的影响。

Influence of magnesium ions on spontaneous opening of DNA base pairs.

作者信息

Every Alicia E, Russu Irina M

机构信息

Department of Chemistry and Molecular Biophysics Program, Wesleyan University, Middletown, Connecticut 06459, USA.

出版信息

J Phys Chem B. 2008 Jun 26;112(25):7689-95. doi: 10.1021/jp8005876. Epub 2008 May 31.

DOI:10.1021/jp8005876
PMID:18512983
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3052203/
Abstract

A large amount of experimental evidence is available for the effects of magnesium ions on the structure and the stability of the DNA double helix. Less is known, however, on how these ions affect the dynamics of the molecule and the stability of each individual base pair. The present work addresses these questions by a study of the DNA duplex [dCGCAGATCTGCG]2, and its interactions with magnesium ions using nuclear magnetic resonance (NMR) spectroscopy and proton exchange. Two-dimensional NMR experiments indicate that binding of magnesium to this DNA duplex does not affect its structure. However, even in the absence of structural changes, magnesium ions specifically affect the exchange properties of imino protons in the four GC/CG base pairs that are located in the interior of the double helix. These specific changes do not result from alterations in the rates of spontaneous opening of these base pairs. Instead, the changes most likely reflect an enhancement in the energetic propensity for spontaneous opening of the GC/CG base pairs that is induced by the binding of magnesium ions.

摘要

关于镁离子对DNA双螺旋结构和稳定性的影响,已有大量实验证据。然而,对于这些离子如何影响分子动力学以及每个碱基对的稳定性,人们了解较少。本研究通过对DNA双链体[dCGCAGATCTGCG]2及其与镁离子的相互作用进行核磁共振(NMR)光谱和质子交换研究,来解决这些问题。二维NMR实验表明,镁与该DNA双链体的结合不会影响其结构。然而,即使在没有结构变化的情况下,镁离子也会特异性地影响位于双螺旋内部的四个GC/CG碱基对中亚氨基质子的交换特性。这些特定变化并非由这些碱基对自发打开速率的改变引起。相反,这些变化很可能反映了镁离子结合诱导的GC/CG碱基对自发打开的能量倾向增强。