首页> 外文期刊>Journal of Molecular Biology >SOLUTION STRUCTURE OF THE OXYTRICHA TELOMERIC REPEAT D[G(4)(T(4)G(4))(3)] G-TETRAPLEX
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SOLUTION STRUCTURE OF THE OXYTRICHA TELOMERIC REPEAT D[G(4)(T(4)G(4))(3)] G-TETRAPLEX

机译:厚朴的端粒重复序列D [G(4)(T(4)G(4))(3)] G-TETRAPLEX的溶液结构

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The solution structure of Oxytricha telomere sequence d[G(4)(T(4)G(4))(3)] in 0.1 M Na+ containing solution has been determined using a combined NMR-molecular dynamics approach including relaxation matrix refinement. This four G(4) repeat sequence folds intramolecularly into a right-handed G-tetraplex containing four stacked G-tetrads which are connected by two lateral T-4 loops and a central diagonal T-4 loop. The guanine glycosidic bonds adopt a syn-anti alternation along the full length of the d[G(4)(T(4)G(4))(3)] sequence while the orientation around adjacent G-tetrads switches between syn . syn . anti . anti and anti . anti . syn . syn alignments. Four distinct grooves are formed by the parallel (two of medium width) and anti-parallel (one wide and one narrow width) alignment of adjacent G-G-G-G segments in the G-tetraplex. The T-4 residues in the diagonal loop are well-defined while the T-4 residues in both lateral loops are under-defined and sample multiple conformations. The solution structure of the Na+-stabilized Oxytricha d[G(4)(T(4)G(4))(3)] G-tetraplex and an earlier solution structure reported from our laboratory on the Na+-stabilized human d[AG(3)(T(2)AG(3))(3)] G-tetraplex exhibit a common folding topology defined by the same syn/anti distribution of guanine residues along individual strands and around individual G-tetrads, as well as a common central diagonal loop which defines the strand directionalities. The well-resolved proton NMR spectra associated with the d[G(4)(T(4)G(4))(3)] G-tetraplex opens the opportunity for studies ranging from cation-dependent characterization of G-tetraplex conformation and hydration to ligand and protein recognition of the distinct grooves associated with this folding topology. (C) 1995 Academic Press Limited [References: 57]
机译:Oxytricha端粒序列d [G(4)(T(4)G(4))(3)]在含0.1 M Na +的溶液中的溶液结构已使用包括弛豫矩阵精炼在内的NMR-分子动力学方法进行了测定。这四个G(4)重复序列分子内折叠成右旋G-四联体,其中包含四个堆叠的G-四联体,它们通过两个侧向T-4环和一个中央对角线T-4环连接。鸟嘌呤糖苷键沿d [G(4)(T(4)G(4))(3)]序列的全长采用顺反交替,而相邻G-tetrads周围的方向在syn之间切换。同步反。反和反。反。同步同步对齐。通过G四联体中相邻G-G-G-G段的平行(中等宽度的两个)和反平行(一个宽和一个窄的宽度)对齐,形成四个不同的凹槽。对角环中的T-4残基定义明确,而两个侧环中的T-4残基定义不明确,并采样了多种构象。 Na +稳定的Oxytricha d [G(4)(T(4)G(4))(3)] G-四链体的溶液结构和我们实验室针对Na +稳定的人d [AG]报告的较早溶液结构(3)(T(2)AG(3))(3)] G-四联体表现出共同的折叠拓扑结构,该结构由鸟嘌呤残基沿单个链和围绕单个G-tetrad的相同顺/反分布定义,以及共同的中央对角线环,它定义了线的方向。与d [G(4)(T(4)G(4))(3)] G-四链体相关的良好解析的质子NMR光谱为研究范围从阳离子依赖的G-四链体构象和与该折叠拓扑相关的独特凹槽的配体水合和蛋白质识别。 (C)1995 Academic Press Limited [参考:57]

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