异头DNA四联体。

Natalia A Kolganova, Anna M Varizhuk, Roman A Novikov, Vladimir L Florentiev, Galina E Pozmogova, Olga F Borisova, Anna K Shchyolkina, Igor P Smirnov, Dmitry N Kaluzhny, Edward N Timofeev
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引用次数: 13

摘要

凝血酶结合适体(TBA)是一种有效抑制凝血酶的15-nt DNA低聚体。结果表明,TBA可折叠成反平行的单分子g -四联体。它的三维椅子状结构由两个由TT和TGT环连接的g四分体组成。TBA在体内被核酸酶快速降解。为了提高TBA对核酸酶的抗性,人们提出了许多修饰的类似物。在这里,我们描述了TBA的端粒修饰。用非天然α异头取代环和核中的选定核苷酸。在T4和T13处对TT环进行了明显的四联体稳定化处理。核心鸟嘌呤的替换可以阻止四重体的组装或诱导g -四分体的重排。发现嵌合适体的抗凝血特性只有在TT环完整的情况下才能保留。相反,TGT环的修饰可以显著提高嵌合适体的核酸酶抗性,而不会显著影响其抗凝血活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Anomeric DNA quadruplexes.

Thrombin-binding aptamer (TBA) is a 15-nt DNA oligomer that efficiently inhibits thrombin. It has been shown that TBA folds into an anti-parallel unimolecular G-quadruplex. Its three-dimensional chair-like structure consists of two G-tetrads connected by TT and TGT loops. TBA undergoes fast degradation by nucleases in vivo. To improve the nuclease resistance of TBA, a number of modified analogs have been proposed. Here, we describe anomeric modifications of TBA. Non-natural α anomers were used to replace selected nucleotides in the loops and core. Significant stabilization of the quadruplex was observed for the anomeric modification of TT loops at T4 and T13. Replacement of the core guanines either prevents quadruplex assembly or induces rearrangement in G-tetrads. It was found that the anticoagulant properties of chimeric aptamers could be retained only with intact TT loops. On the contrary, modification of the TGT loop was shown to substantially increase nuclease resistance of the chimeric aptamer without a notable disturbance of its anticoagulant activity.

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