首页> 外文期刊>Nucleic Acids Research >MINOR GROOVE HYDRATION OF DNA IN AQUEOUS SOLUTION - SEQUENCE-DEPENDENT NEXT NEIGHBOR EFFECT OF THE HYDRATION LIFETIMES IN D(TTAA)(2) SEGMENTS MEASURED BY NMR SPECTROSCOPY
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MINOR GROOVE HYDRATION OF DNA IN AQUEOUS SOLUTION - SEQUENCE-DEPENDENT NEXT NEIGHBOR EFFECT OF THE HYDRATION LIFETIMES IN D(TTAA)(2) SEGMENTS MEASURED BY NMR SPECTROSCOPY

机译:水溶液中DNA的微小凹槽水合-NMR光谱法测定D(TTAA)(2)段中水合生命时间的依序依存的近邻效应

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The hydration in the minor groove of double stranded DNA fragments containing the sequences 5'-dTTAAT, 5'-dTTAAC, 5'-dTTAAA and 5'-dTTAAG was investigated by studying the decanucleotide duplex d(GCATTAATGC)(2) and the singly cross-linked decameric duplexes 5'-d(GCATTAACGC)-3'-linker-5'-d(GCGTTAATGC)-3' and 5'-d(GCCTTAAAGC)-3'-linker-5'-d(GCTTTAAGGC)-3' by NMR spectroscopy. The linker employed consisted of six ethyleneglycol units. The hydration water was detected by NOEs between water and DNA protons in NOESY and ROESY spectra. NOE-NOESY and ROE-NOESY experiments were used to filter out intense exchange cross-peaks and to observe water-DNA NOEs with sugar 1' protons, Positive NOESY cross-peaks corresponding to residence times longer than similar to 0.5 ns were observed for 2H resonances of the central adenine residues in the duplex containing the sequences 5'-dTTAAT and 5'-dTTAAC, but not in the duplex containing the sequences 5'-dTTAAA and 5'-dTTAAG. In all nucleotide sequences studied here, the hydration water in the minor groove is significantly more mobile at both ends of the AT-rich inner segments, as indicated by very weak or negative water-A 2H NOESY cross-peaks, No positive NOESY cross-peaks were detected with the G 1'H and C 1'H resonances, indicating that the minor groove hydration water near GC base pairs is kinetically less restrained than for AT-rich DNA segments, Kinetically stabilized minor groove hydration water was manifested by positive NOESY cross-peaks with both A 2H and 1'H signals of the 5'-dTTAA segment in d(GCATTAATGC)(2). More rigid hydration water was detected near T4 in d(GCATTAATGC)(2) as compared with 5'-d(GCATTAACGC)-3'-linker-5'-d(GCGTTAATGC)-3', although the sequences differ only in a single base pair. This illustrates the high sensitivity of water-DNA NOEs towards small conformational differences.
机译:通过研究十核苷酸双链体d(GCATTAATGC)(2)和单独研究包含序列5'-dTTAAT,5'-dTTAAC,5'-dTTAAA和5'-dTTAAG的双链DNA片段的小沟中的水合。交联的十聚体双链体5'-d(GCATTAACGC)-3'-接头-5'-d(GCGTTAATGC)-3'和5'-d(GCCTTAAAGC)-3'-接头-5'-d(GCTTTAAGGC)-通过NMR光谱法的3'。所用的接头由六个乙二醇单元组成。通过NOESY和ROESY光谱中水和DNA质子之间的NOE检测水合水。 NOE-NOESY和ROE-NOESY实验用于过滤强烈的交换交叉峰,并观察带有糖1'质子的水-DNA NOE,对于2H观察到对应于停留时间长于0.5 ns的正NOESY交叉峰。在含有序列5'-dTTAAT和5'-dTTAAC的双链体中的中央腺嘌呤残基的共振,但在含有序列5'-dTTAAA和5'-dTTAAG的双链体中不存在。在此处研究的所有核苷酸序列中,小槽中的水合水在富含AT的内部区段的两端流动性明显增强,这表明水非常弱或为负-A 2H NOESY交叉峰,没有正NOESY交叉峰。检测到具有G 1'H和C 1'H共振的峰,表明GC碱基对附近的小沟水合水在动力学上比富含AT的DNA片段受动力学抑制小,运动稳定的小沟水合水表现为正NOESY d(GCATTAATGC)(2)中具有5'-dTTAA段的A 2H和1'H信号的交叉峰。与5'-d(GCATTAACGC)-3'-linker-5'-d(GCGTTAATGC)-3'相比,在d(GCATTAATGC)(2)的T4附近检测到了更多的刚性水。单碱基对。这说明了水-DNA NOE对小的构象差异的高度敏感性。

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