Department of Chemistry and the Center for Cell and Genome Science, University of Utah, Salt Lake City, Utah 84112, United States.
J Am Chem Soc. 2011 Aug 17;133(32):12426-9. doi: 10.1021/ja205518e. Epub 2011 Jul 22.
Here we describe the first use of small-molecule binding to direct a chemical reaction between two nucleic acid strands. The reported reaction is a ligation between two fragments of a DNA split aptamer using strain-promoted azide-alkyne cycloaddition. Utilizing the split aptamer for cocaine, we demonstrate small-molecule-dependent ligation that is dose-dependent over a wide range of cocaine concentrations and is compatible with complex biological fluids such as human blood serum. Moreover, studies of split aptamer ligation at varying salt concentrations and using structurally similar analogues of cocaine have revealed new insight into the assembly and small-molecule binding properties of the cocaine split aptamer. The ability to translate the presence of a small-molecule target into the output of DNA ligation is anticipated to enable the development of new, broadly applicable small-molecule detection assays.
在这里,我们描述了小分子结合首次用于指导两个核酸链之间的化学反应。报道的反应是使用应变促进的叠氮-炔环加成反应连接 DNA 分裂适体的两个片段。利用分裂适体检测可卡因,我们证明了小分子依赖性连接,在广泛的可卡因浓度范围内具有剂量依赖性,并且与复杂的生物流体如人血清兼容。此外,对不同盐浓度下的分裂适体连接以及使用可卡因的结构类似物进行的研究,揭示了可卡因分裂适体的组装和小分子结合特性的新见解。将小分子靶标的存在转化为 DNA 连接的输出的能力有望为新的、广泛适用的小分子检测方法的开发提供支持。