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Science 30 August 1991:
Vol. 253. no. 5023, pp. 1019 - 1022
DOI: 10.1126/science.1887215

Articles

Science, Vol 253, Issue 5023, 1019-1022
Copyright © 1991 by American Association for the Advancement of Science


articles

Medium effects in antibody-catalyzed reactions

C Lewis, T Kramer, S Robinson, and D Hilvert

Department of Chemistry, Research Institute of Scripps Clinic, La Jolla, CA 92037.

Catalytic antibody technology has been used to explore the contribution of medium effects to the overall rate of an enzyme-catalyzed reaction. An antibody generated against a derivative of 2-acetamido-1,5-napthalenedisulfonate efficiently catalyzes the decarboxylation of 5-nitro-3-carboxybenzisoxazole. This unimolecular reaction is not susceptible to general acid-base catalysis but is highly sensitive to microenvironment; thus, it provides a simple chemical model for biologically important decarboxylations. The 10(4)-fold rate acceleration observed for the antibody reflects the kinetic advantage of the low-dielectric environment of the binding pocket acting to destabilize the substrate by desolvation and to stabilize the charge-delocalized transition state through dispersion interactions. These results are pertinent to an understanding of solvent effects in enzymic reactions in general and suggest approaches for developing antibody catalysts for numerous other reactions that involve large changes in charge distribution as the reaction coordinate is traversed.


THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
Evolution of Shape Complementarity and Catalytic Efficiency from a Primordial Antibody Template.
J. Xu, Q. Deng, J. Chen, K. N. Houk, J. Bartek, D. Hilvert, and I. A. Wilson (1999)
Science 286, 2345-2348
   Abstract »    Full Text »
Antibody catalysis of a disfavored chemical transformation.
K. Janda, C. Shevlin, and R. Lerner (1993)
Science 259, 490-493
   Abstract »    PDF »



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Science. ISSN 0036-8075 (print), 1095-9203 (online)