Enhancing Catalytic Activity of Uranyl-Dependent DNAzyme by Flexible Linker Insertion for More Sensitive Detection of Uranyl IonClick to copy article linkArticle link copied!
- Mengli FengMengli FengDepartment of Chemistry, Beijing Key Laboratory for Microanalytical Methods and Instrumentation, Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (Ministry of Education), Tsinghua University, Beijing 100084, People’s Republic of ChinaMore by Mengli Feng
- Chunmei GuChunmei GuDepartment of Chemistry, Beijing Key Laboratory for Microanalytical Methods and Instrumentation, Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (Ministry of Education), Tsinghua University, Beijing 100084, People’s Republic of ChinaMore by Chunmei Gu
- Yanping SunYanping SunSchool of Chemistry and Biological Engineering, University of Science and Technology Beijing, Beijing 100083, People’s Republic of ChinaMore by Yanping Sun
- Shuyuan ZhangShuyuan ZhangSchool of Chemistry and Biological Engineering, University of Science and Technology Beijing, Beijing 100083, People’s Republic of ChinaMore by Shuyuan Zhang
- Aijun TongAijun TongDepartment of Chemistry, Beijing Key Laboratory for Microanalytical Methods and Instrumentation, Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (Ministry of Education), Tsinghua University, Beijing 100084, People’s Republic of ChinaMore by Aijun Tong
- Yu Xiang*Yu Xiang*E-mail for Y.X.: [email protected]Department of Chemistry, Beijing Key Laboratory for Microanalytical Methods and Instrumentation, Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (Ministry of Education), Tsinghua University, Beijing 100084, People’s Republic of ChinaMore by Yu Xiang
Abstract

The uranyl-dependent DNAzyme 39E cleaves its nucleic acid substrate in the presence of uranyl ion (UO22+). It has been widely utilized in many sensor designs for selective and sensitive detection of UO22+ in the environment and inside live cells. In this work, by inserting a flexible linker (C3 Spacer) into one critical site (A20) of the 39E catalytic core, we successfully enhanced the original catalytic activity of 39E up to 8.1-fold at low UO22+ concentrations. Applying such a modified DNAzyme (39E-A20-C3) in a label-free fluorescent sensor for UO22+ detection achieved more than 1 order of magnitude sensitivity enhancement over using native 39E, with the UO22+ detection limit improved from 2.6 nM (0.63 ppb) to 0.19 nM (0.047 ppb), while the high selectivity to UO22+ over other metal ions was fully preserved. The method was also successfully applied for the detection of UO22+-spiked environmental water samples to demonstrate its practical usefulness.
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