Probing Metal-Dependent Phosphate Binding for the Catalysis of the 17E DNAzyme

Woohyun J. Moon, Po‐Jung Jimmy Huang, Juewen Liu, Woohyun J. Moon, Po‐Jung Jimmy Huang, Juewen Liu


Abstract
The 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.
Cite:
Woohyun J. Moon, Po‐Jung Jimmy Huang, Juewen Liu, Woohyun J. Moon, Po‐Jung Jimmy Huang, and Juewen Liu. 2021. Probing Metal-Dependent Phosphate Binding for the Catalysis of the 17E DNAzyme. Biochemistry, Volume 60, Issue 24, 60(24):1909–1918.
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