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由Sr2+稳定的凝血酶结合DNA适配体的核磁共振结构。

NMR structure of the thrombin-binding DNA aptamer stabilized by Sr2+.

作者信息

Mao X, Marky L A, Gmeiner W H

机构信息

Department of Biochemistry, Wake Forest University School of Medicine, Winston-Salem, NC 27157-1016, USA.

出版信息

J Biomol Struct Dyn. 2004 Aug;22(1):25-33. doi: 10.1080/07391102.2004.10506977.

Abstract

The structure of thrombin-binding DNA aptamer complexed with a single Sr2+ ion (Sr2+:TBA complex) has been determined using NMR spectroscopy and restrained molecular dynamics simulations. The quadruplex structure for the Sr2+:TBA complex is similar in topology, but distinct in structure, from that previously reported for the K+:TBA complex. The inter-tetrad distance of the Sr2+:TBA complex is 3.8 angstroms, or 0.7 angstroms larger than in the K+:TBA complex. This substantial difference can be attributed to a different binding site for Sr2+ in the Sr2+:TBA complex than for K+ in the K+:TBA complex. The Sr2+:TBA complex assumes a 1:1 stoichiometry, and it is very likely that the Sr2+ ion simultaneously interacts with the eight O6 atoms of the two G-tetrads. The results indicate that quadruplex DNA structures are highly sensitive to the presence of specific metal ions. The binding of specific metal ions may modulate the biological activity of quadruplex DNA structures in vivo.

摘要

已使用核磁共振光谱法和受限分子动力学模拟确定了与单个Sr2+离子复合的凝血酶结合DNA适体复合物(Sr2+:TBA复合物)的结构。Sr2+:TBA复合物的四链体结构在拓扑结构上与先前报道的K+:TBA复合物相似,但在结构上有所不同。Sr2+:TBA复合物的四联体间距离为3.8埃,比K+:TBA复合物中的大四联体间距离大0.7埃。这种显著差异可归因于Sr2+:TBA复合物中Sr2+的结合位点与K+:TBA复合物中K+的结合位点不同。Sr2+:TBA复合物的化学计量比为1:1,并且Sr2+离子很可能同时与两个G-四联体的八个O6原子相互作用。结果表明,四链体DNA结构对特定金属离子的存在高度敏感。特定金属离子的结合可能会调节体内四链体DNA结构的生物活性。

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