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. 1989 Mar;86(6):1746-50.
doi: 10.1073/pnas.86.6.1746.

On the mechanism of action of ribonucleases: dinucleotide cleavage catalyzed by imidazole and Zn2+

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On the mechanism of action of ribonucleases: dinucleotide cleavage catalyzed by imidazole and Zn2+

R Breslow et al. Proc Natl Acad Sci U S A. 1989 Mar.

Abstract

Cyclization/cleavage of the 2-(p-nitrophenyl) phosphate ester of propylene glycol is catalyzed by imidazole and, much more effectively, by Zn2+ with imidazole. In the latter case, the mechanism involves simultaneous Lewis acid/base catalysis. Similar Zn2+ and imidazole catalysis of cyclization/cleavage is seen with the dinucleotide 3',5'-UpU (uridylyluridine). Again, the zinc system is much more effective than is catalysis by imidazole alone, and in this case simultaneous Lewis acid/base catalysis substitutes for the sequential proton acid/base catalysis seen with polynucleotides or dinucleotides and imidazole buffer catalysts. A mechanism is proposed for catalysis of RNA cleavage by the enzyme ribonuclease A, and the relationship of that mechanism to the action of the enzyme model systems is discussed.

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References

    1. Anal Biochem. 1985 Feb 1;144(2):563-8 - PubMed
    1. Biochemistry. 1971 May 25;10(11):2014-9 - PubMed

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