Saito Ken, Shimada Naohiko, Maruyama Atushi
Department of Life Science and Technology, Tokyo Institute of Technology , Yokohama , Japan.
Sci Technol Adv Mater. 2016 Jul 29;17(1):437-442. doi: 10.1080/14686996.2016.1208627. eCollection 2016.
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'--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.
具有RNA切割活性的脱氧核酶(DNAzyme)已被广泛探索用作治疗和诊断工具。为了提高DNAzyme的整体活性,化学切割步骤和周转步骤都应得到改进。我们已经表明,阳离子共聚物通过提高周转效率增强了DNAzyme活性。本文研究了该共聚物对用锁核酸(LNA)或2'-甲基化(2'-OMe)核酸修饰的DNAzyme的影响。该共聚物提高了这些化学修饰的DNAzyme的活性。在共聚物存在下,2'-OMe修饰的DNAzyme的多周转催化活性提高了30倍以上。通过添加的共聚物与DNAzyme的化学修饰协同作用,成功提高了DNAzyme的催化活性。