Huang Po-Jung Jimmy, Liu Juewen
Department of Chemistry, Waterloo Institute for Nanotechnology, University of Waterloo , 200 University Avenue West, Waterloo, Ontario Canada , N2L 3G1.
Anal Chem. 2014 Jun 17;86(12):5999-6005. doi: 10.1021/ac501070a. Epub 2014 Jun 3.
Cadmium, mercury, and lead are collectively banned by many countries and regions in electronic devices due to their extremely high toxicity. To date, no sensing method can detect them as a group and also individually with sufficient sensitivity and selectivity. An RNA-cleaving DNAzyme (Ce13d) was recently reported to be active with trivalent lanthanides, which are hard Lewis acids. In this work, phosphorothioate (PS) modifications were systematically made on Ce13d. A single PS modification at the substrate cleavage site shifts the activity from being dependent on lanthanides to soft thiophilic metals. By incorporating the PS modification to another DNAzyme, a sensor array was prepared to detect each metal. Individual sensors have excellent sensitivity (limit of detection = 4.8 nM Cd(2+), 2.0 nM Hg(2+), and 0.1 nM Pb(2+)). This study provides a new route to obtain metal-specific DNAzymes by atomic replacement and also offers important mechanistic insights into metal binding and DNAzyme catalysis.
由于镉、汞和铅具有极高的毒性,许多国家和地区已对其在电子设备中的使用进行了全面禁止。到目前为止,尚无检测方法能够同时对它们进行分组检测,并分别实现足够的灵敏度和选择性。最近有报道称,一种能够切割RNA的脱氧核酶(Ce13d)对作为硬路易斯酸的三价镧系元素具有活性。在本研究中,我们对Ce13d进行了系统的硫代磷酸酯(PS)修饰。在底物切割位点进行单一PS修饰后,其活性从依赖镧系元素转变为依赖软亲硫金属。通过将PS修饰整合到另一种脱氧核酶中,制备了一种传感器阵列用于检测每种金属。单个传感器具有出色的灵敏度(检测限分别为4.8 nM Cd(2+)、2.0 nM Hg(2+)和0.1 nM Pb(2+))。本研究提供了一种通过原子置换获得金属特异性脱氧核酶的新途径,并为金属结合和脱氧核酶催化提供了重要的机制见解。