首页> 外文OA文献 >The internal dynamics of mini c TAR DNA probed by electron paramagnetic resonance of nitroxide spin-labels at the lower stem, the loop, and the bulge.
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The internal dynamics of mini c TAR DNA probed by electron paramagnetic resonance of nitroxide spin-labels at the lower stem, the loop, and the bulge.

机译:mini c TAR DNA的内部动力学由下部茎,环和凸起处的一氧化氮自旋标记的电子顺磁共振探测。

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摘要

Electron paramagnetic resonance (EPR) at 236.6 and 9.5 GHz probed the tumbling of nitroxide spin probes in the lower stem, in the upper loop, and near the bulge of mini c TAR DNA. High-frequency 236.6 GHz EPR, not previously applied to spin-labeled oligonucleotides, was notably sensitive to fast, anisotropic, hindered local rotational motion of the spin probe, occurring approximately about the NO nitroxide axis. Labels attached to the 2'-aminocytidine sugar in the mini c TAR DNA showed such anisotropic motion, which was faster in the lower stem, a region previously thought to be partially melted. More flexible labels attached to phosphorothioates at the end of the lower stem tumbled isotropically in mini c TAR DNA, mini TAR RNA, and ψ(3) RNA, but at 5 °C, the motion became more anisotropic for the labeled RNAs, implying more order within the RNA lower stems. As observed by 9.5 GHz EPR, the slowing of nanosecond motions of large segments of the oligonucleotide was enhanced by increasing the ratio of the nucleocapsid protein NCp7 to mini c TAR DNA from 0 to 2. The slowing was most significant at labels in the loop and near the bulge. At a 4:1 ratio of NCp7 to mini c TAR DNA, all labels reported tumbling times of >5 ns, indicating a condensation of NCp7 and TAR DNA. At the 4:1 ratio, pulse dipolar EPR spectroscopy of bilabels attached near the 3' and 5' termini showed evidence of an NCp7-induced increase in the 3'-5' end-to-end distance distribution and a partially melted stem.
机译:236.6和9.5 GHz的电子顺磁共振(EPR)探测了下茎,上环和mini c TAR DNA凸起附近的一氧化氮自旋探针的翻滚。高频236.6 GHz EPR,以前未应用于自旋标记的寡核苷酸,对旋转探针的快速,各向异性,受阻局部旋转运动非常敏感,大约在NO氮氧化物轴附近发生。附着在微型c TAR DNA中2'-氨基胞苷糖上的标记显示出这种各向异性运动,在下部茎干中较快地运动,该下部茎先前被认为部分熔化。附着在下部茎末端硫代磷酸酯上的更灵活的标记在mini c TAR DNA,mini TAR RNA和ψ(3)RNA中各向同性地滚动,但在5°C时,标记RNA的运动变得更加各向异性,这意味着更多RNA下茎内部有序。如9.5 GHz EPR所观察到的,通过将核衣壳蛋白NCp7与mini c TAR DNA的比例从0增加到2,增强了寡核苷酸大片段纳秒运动的减慢。在隆起附近。在NCp7与mini c TAR DNA的比率为4:1时,所有标记的翻转时间均大于5 ns,表明NCp7和TAR DNA发生了缩合。在4:1的比率下,连接在3'和5'末端附近的双标签的脉冲偶极EPR光谱显示了NCp7诱导的3'-5'端对端距离分布增加和茎部分融化的证据。

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