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Substrate specificity of an active dinuclear Zn(II) catalyst for cleavage of RNA analogues and a dinucleoside.

O'Donoghue, A. M. C. and Pyun, S. Y. and Yang, M.-Y. and Morrow, J. R. and Richard, J. P. (2006) 'Substrate specificity of an active dinuclear Zn(II) catalyst for cleavage of RNA analogues and a dinucleoside.', Journal of the American Chemical Society., 128 (5). pp. 1615-1621.

Abstract

The cleavage of the diribonucleoside UpU (uridylyl-3'-5'-uridine) to form uridine and uridine (2',3')-cyclic phosphate catalyzed by the dinuclear Zn(II) complex of 1,3-bis(1,4,7-triazacyclonon-1-yl)-2-hydroxypropane (Zn2(1)(H2O)) has been studied at pH 7-10 and 25 C. The kinetic data are consistent with the accumulation of a complex between catalyst and substrate and were analyzed to give values of kc (s-1), Kd (M), and kc/Kd (M-1 s-1) for the Zn2(1)(H2O)-catalyzed reaction. The pH rate profile of values for log kc/Kd for Zn2(1)(H2O)-catalyzed cleavage of UpU shows the same downward break centered at pH 7.8 as was observed in studies of catalysis of cleavage of 2-hydroxypropyl-4-nitrophenyl phosphate (HpPNP) and uridine-3'-4-nitrophenyl phosphate (UpPNP). At low pH, where the rate acceleration for the catalyzed reaction is largest, the stabilizing interaction between Zn2(1)(H2O) and the bound transition states is 9.3, 7.2, and 9.6 kcal/mol for the catalyzed reactions of UpU, UpPNP, and HpPNP, respectively. The larger transition-state stabilization for Zn2(1)(H2O)-catalyzed cleavage of UpU (9.3 kcal/mol) compared with UpPNP (7.2 kcal/mol) provides evidence that the transition state for the former reaction is stabilized by interactions between the catalyst and the C-5'-oxyanion of the basic alkoxy leaving group.

Item Type:Article
Full text:Full text not available from this repository.
Publisher Web site:http://dx.doi.org/10.1021/ja056167f
Record Created:22 Feb 2008
Last Modified:08 Apr 2009 16:30

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