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Publication Additional Information Download
Publication Type
Journal Article
Authorship
Woohyun J. Moon, Po-Jung Jimmy Huang and Juewen Liu
Title
Probing Metal-dependent Phosphate Binding for the Catalysis of the 17E DNAzyme
Year
2021
Publication Outlet
Biochemistry, 60, 1909-1918
DOI
https://doi.org/10.1021/acs.biochem.1c00091
Citation
Woohyun J. Moon, Po-Jung Jimmy Huang and Juewen Liu, Probing Metal-dependent Phosphate Binding for the Catalysis of the 17E DNAzyme, Biochemistry, 60, 1909-1918, https://doi.org/10.1021/acs.biochem.1c00091 , 2021
Abstract
he RNA-cleaving 17E DNAzyme exhibits different levels of cleavage activity in the presence of various divalent metal ions, with Pb2+ giving the fastest cleavage. In this study, the metal–phosphate interaction is probed to understand the trend of activity with different metal ions. For the first-row transition metals, the lowest activity shown by Ni2+ correlates with the inhibition by the inorganic phosphate and its water ligand exchange rate, suggesting inner-sphere metal coordination. Cleavage activity with the two stereoisomers of the phosphorothioate-modified substrates, Rp and Sp, indicated that Mg2+, Mn2+, Fe2+, and Co2+ had the highest Sp:Rp activity ratio of >900. Comparatively, the activity was much less affected using the thiophilic metals, including Pb2+, suggesting inner-sphere coordination. The pH–rate profiles showed that Pb2+ was different than the rest of the metal ions in having a smaller slope and a similar fitted apparent pKa and the pKa of metal-bound water. Combining previous reports and our current results, we propose that Pb2+ most likely plays the role of a general acid while the other metal ions are Lewis acid catalysts interacting with the scissile phosphate.
Program Affiliations
GWF: Global Water Futures
Project Affiliations
GWF-SSSWQM: Sensors and Sensing Systems for Water Quality Monitoring
Publication Stage
Published
Additional Information
Sensor and Sensing Systems for Water Quality Monitoring 2, Refereed Publications
Download Links
https://doi.org/10.1021/acs.biochem.1c00091
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