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二价金属阳离子与嘌呤的N7配位时,由于Hoogsteen型氢键增强程度不同,会以不同方式稳定PyPuPu DNA三链体。

Divalent metal cations upon coordination to the N7 of purines differentially stabilize the PyPuPu DNA triplex due to unequal Hoogsteen-type hydrogen bond enhancement.

作者信息

Potaman V N, Soyfer V N

机构信息

Biology Department, George Mason University, Fairfax, VA 22030.

出版信息

J Biomol Struct Dyn. 1994 Apr;11(5):1035-40. doi: 10.1080/07391102.1994.10508050.

Abstract

The PyPuPu triplexes consisting of CGG triads are stabilized by alkaline earth cations (Ca2+, Mg2+) and transition metal cations (Mn2+, Co2+, Ni2+, Zn2+, Cd2+), while similar triplexes including TAA triads are stabilized only by transition metal cations. We hypothesize that such a differential triplex stabilization by divalent metal cations can be the consequence of their coordination to the N7 of the third strand purines with concomitant polarization effects on the bases resulting in unequal Hoogsteen-type hydrogen bond enhancement.

摘要

由CGG三联体组成的PyPuPu三链体通过碱土金属阳离子(Ca2+、Mg2+)和过渡金属阳离子(Mn2+、Co2+、Ni2+、Zn2+、Cd2+)得以稳定,而包括TAA三联体在内的类似三链体仅通过过渡金属阳离子来稳定。我们推测,二价金属阳离子对三链体的这种差异性稳定作用可能是由于它们与第三条链嘌呤的N7配位,并伴随对碱基的极化效应,从而导致Hoogsteen型氢键增强不均等。

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