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Cooperative enhancement of deoxyribozyme activity by chemical modification and added cationic copolymer

机译:通过化学修饰和添加阳离子共聚物协同增强脱氧核酶活性

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摘要

Deoxyribozymes (DNAzymes) having RNA-cleaving activity have widely been explored as tools for therapeutic and diagnostic purposes. Both the chemical cleaving step and the turnover step should be improved for enhancing overall activity of DNAzymes. We have shown that cationic copolymer enhanced DNAzyme activity by increasing turnover efficacy. In this paper, effects of the copolymer on DNAzymes modified with locked nucleic acids (LNA) or 2′-O-methylated (2′-OMe) nucleic acids were studied. The copolymer increased activity of these chemically modified DNAzymes. More than 30-fold enhancement in multiple-turnover catalytic activity was observed with 2′-OMe-modified DNAzyme in the presence of the copolymer. DNAzyme catalytic activity was successfully enhanced by cooperation of the added copolymer and chemical modification of DNAzyme.
机译:具有RNA切割活性的脱氧核酶(DNA核酶)已被广泛用作治疗和诊断目的的工具。化学裂解步骤和周转步骤均应改善,以增强DNA酶的整体活性。我们已经表明,阳离子共聚物通过提高周转效率来增强DNA酶的活性。本文研究了共聚物对锁核酸(LNA)或2'-O-甲基化(2'-OMe)核酸修饰的DNA酶的影响。共聚物增加了这些化学修饰的DNA酶的活性。在共聚物的存在下,用2'-OMe-修饰的DNAzyme观察到多转化催化活性提高了30倍以上。通过添加的共聚物和DNAzyme的化学修饰,成功地增强了DNAzyme的催化活性。

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