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Energetics and kinetics of a conformational switch in G-quadruplex DNA

机译:G-四链体DNa中构象转换的能量学和动力学

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摘要

Circular dichroism and differential scanning calorimetry were used to determine the energetics of the conformational switch of the human telomere quadruplex formed by the sequence d[AGGG(TTAGGG)3] between the sodium basket form and the potassium hybrid form. The energy barrier separating the two conformations was found to be modest, only 1.4-2.4 kcal mol(-1). The kinetics of exchange of bound K+ for Na+ cations and the concomitant conformational switch was assessed by measuring time-dependent changes in the circular dichroism spectrum accompanying the cation exchange reaction. The time course of these changes was found to consist of three distinct kinetic processes: a rapid phase that was complete in less than 5 ms followed by two slower phases with relaxation times of 40-50 s and 600-800 s at 25 degrees C and pH 7.0. We interpret these kinetics in terms of a model in which the bound Na+ cations are rapidly replaced by K+ followed by relatively slow structural rearrangements to generate the final K(+)-bound product(s). Circular dichroism studies showed that addition of the porphyrin TmPyP4 promoted conversion of the basket to the hybrid form. The kinetics of the TmPyP4-induced conformational change were the same as those observed for the cation exchange reaction.
机译:使用圆二色性和差示扫描量热法确定钠篮子形式和钾杂化形式之间由序列d [AGGG(TTAGGG)3]形成的人端粒四链体构象转换的能量。发现分隔两个构象的能垒适度,只有1.4-2.4 kcal mol(-1)。通过测量伴随阳离子交换反应的圆二色性光谱随时间的变化来评估结合的K +交换Na +阳离子和伴随的构象转换的动力学。发现这些变化的时间过程包括三个截然不同的动力学过程:一个在不到5 ms的时间内完成的快速相,然后是两个较慢的相,它们在25摄氏度和40摄氏度下的弛豫时间分别为40-50 s和600-800 s。 pH值7.0。我们用一个模型来解释这些动力学,在该模型中,结合的Na +阳离子迅速被K +取代,然后进行相对缓慢的结构重排,以生成最终的K(+)结合产物。圆二色性研究表明,添加卟啉TmPyP4可以促进篮子向杂种形式的转化。 TmPyP4诱导的构象变化的动力学与阳离子交换反应所观察到的动力学相同。

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