3'-氨基-2'-O,4'- c -亚甲基桥接核酸修饰促进三联体形成。

Kiyomi Sasaki, S M Abdur Rahman, Norihiro Sato, Satoshi Obika, Takeshi Imanishi, Hidetaka Torigoe
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引用次数: 1

摘要

我们研究了3'-氨基-2'-O,4'- c -亚甲基桥接核酸(3'-氨基-2',4'-BNA)三聚体形成寡核苷酸(TFO)的主链修饰对中性pH下嘧啶基序三聚体形成的影响,在中性pH下嘧啶基序三聚体不稳定。3′-氨基-2′,4′-BNA修饰的TFO在pH 6.8下的熔融温度显著高于未修饰的TFO。TFO的3'-氨基-2',4'-BNA修饰增加了中性ph下嘧啶基序三联体的热稳定性。目前的结果肯定支持TFO的3'-氨基-2',4'-BNA修饰可能是一个关键的化学修饰,并可能最终导致抗原策略在体内治疗应用的进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Promotion of triplex formation by 3'-amino-2'-O,4'-C-methylene bridged nucleic acid modification.

We examined the effect of 3'-amino-2'-O,4'-C-methylene bridged nucleic acid (3'-amino-2',4'-BNA) backbone modification of triplex-forming oligonucleotide (TFO) on the pyrimidine motif triplex formation at neutral pH, a condition where pyrimidine motif triplexes are unstable. The melting temperature of the pyrimidine motif triplex at pH 6.8 with 3'-amino-2',4'-BNA modified TFO was significantly higher than that observed with unmodified TFO. The 3'-amino-2',4'-BNA modification of TFO increased the thermal stability of the pyrimidine motif triplex at neutral pH. The present results certainly support the idea that the 3'-amino-2',4'-BNA modification of TFO could be a key chemical modification and may eventually lead to progress in therapeutic applications of the antigene strategy in vivo.

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