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Highly sensitive self-complementary DNA nanoswitches triggered by polyelectrolytes.

作者信息

Wu Jincai, Yu Feng, Zhang Zheng, Chen Yong, Du Jie

机构信息

College of Materials and Chemistry Engineering, Hainan University, Haikou 570228, China.

出版信息

Nanoscale. 2016 Jan 7;8(1):464-70. doi: 10.1039/c5nr05193b.

DOI:10.1039/c5nr05193b
PMID:26627445
Abstract

Dimerization of two homologous strands of genomic DNA/RNA is an essential feature of retroviral replication. Herein we show that a cationic comb-type copolymer (CCC), poly(L-lysine)-graft-dextran, accelerates the dimerization of self-complementary stem-loop DNA, frequently found in functional DNA/RNA molecules, such as aptamers. Furthermore, an anionic polymer poly(sodium vinylsulfonate) (PVS) dissociates CCC from the duplex shortly within a few seconds. Then single stem-loop DNA spontaneously transforms from its dimer. Thus we can easily control the dimer and stem-loop DNA by switching on/off CCC activity. Both polyelectrolytes and DNA concentrations are in the nanomole per liter range. The polyelectrolyte-assisted transconformation and sequences design strategy ensures the reversible state control with rapid response and effective switching under physiologically relevant conditions. A further application of this sensitive assembly is to construct an aptamer-type drug delivery system, bind or release functional molecules responding to its transconformation.

摘要

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