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一种有助于稳定四分子G-四链体结构的新型嘧啶四联体。

A novel pyrimidine tetrad contributing to stabilize tetramolecular G-quadruplex structures.

作者信息

Esposito V, Pepe A, Filosa R, Mayol L, Virgilio A, Galeone A

机构信息

Department of Pharmacy, University of Naples "Federico II", Via D. Montesano, 49, 80131 Naples, Italy.

Department of Science, University of Basilicata, Viale dell'Ateneo Lucano 10, I-85100, Potenza, Italy.

出版信息

Org Biomol Chem. 2016 Mar 14;14(10):2938-43. doi: 10.1039/c5ob02358k.

DOI:10.1039/c5ob02358k
PMID:26876038
Abstract

G-quadruplex structures formed by oligodeoxyribonucleotides TGGU(NH2)GGT (AM, U(NH2) = 5-amino-2'-deoxyuridine), TGGU(Br)GGT (BR, U(Br) = 5-bromo-2'-deoxyuridine) and TGGTGGT (TH) have been investigated through circular dichroism, nuclear magnetic resonance, gel electrophoresis and molecular modeling techniques. Collected data indicate that all 7-mer oligonucleotides form tetramolecular parallel G-quadruplex structures with all residues adopting anti glycosidic bonds. In the case of AM, data suggest the occurrence of a novel U(NH2)-tetrad characterized by eight hydrogen bonds that stabilizes the G-quadruplex structure more efficiently than U(Br)- and T-tetrads.

摘要

通过圆二色性、核磁共振、凝胶电泳和分子建模技术,对由寡脱氧核糖核苷酸TGGU(NH2)GGT(AM,U(NH2)=5-氨基-2'-脱氧尿苷)、TGGU(Br)GGT(BR,U(Br)=5-溴-2'-脱氧尿苷)和TGGTGGT(TH)形成的G-四链体结构进行了研究。收集的数据表明,所有7聚体寡核苷酸均形成四分子平行G-四链体结构,所有残基均采用反式糖苷键。对于AM,数据表明存在一种新型的U(NH2)-四联体,其特征是有八个氢键,比U(Br)-和T-四联体更有效地稳定G-四链体结构。

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引用本文的文献

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In What Ways Do Synthetic Nucleotides and Natural Base Lesions Alter the Structural Stability of G-Quadruplex Nucleic Acids?合成核苷酸和天然碱基损伤如何改变G-四链体核酸的结构稳定性?
J Nucleic Acids. 2017;2017:1641845. doi: 10.1155/2017/1641845. Epub 2017 Oct 18.