Accelerating Turnover Frequency in Nucleic Acid Templated Reactions

被引:25
作者
Chang, Dalu [1 ]
Kim, Ki Tae [1 ]
Lindberg, Eric [1 ]
Winssinger, Nicolas [1 ]
机构
[1] Univ Geneva, Fac Sci, NCCR Chem Biol, Dept Organ Chem, 30 Quai Ernest Ansermet, CH-1211 Geneva, Switzerland
基金
瑞士国家科学基金会;
关键词
REDUCING PRODUCT INHIBITION; NUCLEOBASE-MODIFIED PNA; MESSENGER-RNA; SIGNAL AMPLIFICATION; LIGATION REACTIONS; CHEMICAL-REACTIONS; DUPLEX FORMATION; LIVE CELLS; IN-VITRO; DNA;
D O I
10.1021/acs.bioconjchem.7b00663
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Nucleic acid templated reactions have attracted attention as an important technology to sense oligonucleotides and to translate nucleic acid-based instructions into diverse outputs. Great progress has been made in accelerating the reaction in order to improve signal amplification, reaching rates where substrate turnover rather than chemical reaction is rate limiting. Herein we explore the utility of architectures inspired by three-way junction that yield a cleavage of a strand thus accelerating substrate turnover. We demonstrate that such design can overcome product inhibition in templated reactions and operate close to the rate of hybridization.
引用
收藏
页码:158 / 163
页数:6
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