Nonspecific medium effects versus specific group positioning in the antibody and albumin catalysis of the base-promoted ring-opening reactions of benzisoxazoles
- PMID: 15225061
- DOI: 10.1021/ja0490727
Nonspecific medium effects versus specific group positioning in the antibody and albumin catalysis of the base-promoted ring-opening reactions of benzisoxazoles
Abstract
The mechanisms by which solvents, antibodies, and albumins influence the rates of base-catalyzed reactions of benzisoxazoles have been explored theoretically. New experimental data on substituent effects and rates of reactions in several solvents, in an antibody, and in an albumin are reported. Quantum mechanical calculations were carried out for the reactions in water and acetonitrile, and docking of the transition state into a homology model of antibody 34E4 and an X-ray structure of human serum albumin was accomplished. A microenvironment made up of catalytic polar groups (glutamate in antibody 34E4 and lysine in human serum albumin) surrounded by relatively nonpolar groups is present in both catalytic proteins.
Similar articles
-
Catalysis on the coastline: theozyme, molecular dynamics, and free energy perturbation analysis of antibody 21D8 catalysis of the decarboxylation of 5-nitro-3-carboxybenzisoxazole.J Comput Chem. 2003 Jan 15;24(1):98-110. doi: 10.1002/jcc.10151. J Comput Chem. 2003. PMID: 12483679
-
Catalysis of decarboxylation by a preorganized heterogeneous microenvironment: crystal structures of abzyme 21D8.J Mol Biol. 2000 Oct 6;302(5):1213-25. doi: 10.1006/jmbi.2000.4503. J Mol Biol. 2000. PMID: 11183784
-
Positional ordering of reacting groups contributes significantly to the efficiency of proton transfer at an antibody active site.J Am Chem Soc. 2005 Feb 2;127(4):1307-12. doi: 10.1021/ja044647l. J Am Chem Soc. 2005. PMID: 15669871
-
The structural and functional basis of antibody catalysis.Annu Rev Biophys Biomol Struct. 1997;26:461-93. doi: 10.1146/annurev.biophys.26.1.461. Annu Rev Biophys Biomol Struct. 1997. PMID: 9241427 Review.
-
Structures and mechanisms of Nudix hydrolases.Arch Biochem Biophys. 2005 Jan 1;433(1):129-43. doi: 10.1016/j.abb.2004.08.017. Arch Biochem Biophys. 2005. PMID: 15581572 Review.
Cited by
-
Optimization of the in-silico-designed kemp eliminase KE70 by computational design and directed evolution.J Mol Biol. 2011 Apr 1;407(3):391-412. doi: 10.1016/j.jmb.2011.01.041. Epub 2011 Jan 28. J Mol Biol. 2011. PMID: 21277311 Free PMC article.
-
Kemp Eliminase Activity of Ketosteroid Isomerase.Biochemistry. 2017 Jan 31;56(4):582-591. doi: 10.1021/acs.biochem.6b00762. Epub 2017 Jan 20. Biochemistry. 2017. PMID: 28045505 Free PMC article.
-
Evaluation and ranking of enzyme designs.Protein Sci. 2010 Sep;19(9):1760-73. doi: 10.1002/pro.462. Protein Sci. 2010. PMID: 20665693 Free PMC article.
-
Bovine serum albumin-catalyzed deprotonation of [1-(13)C]glycolaldehyde: protein reactivity toward deprotonation of the alpha-hydroxy alpha-carbonyl carbon.Biochemistry. 2010 Sep 7;49(35):7704-8. doi: 10.1021/bi101118g. Biochemistry. 2010. PMID: 20687575 Free PMC article.
-
Design of a switchable eliminase.Proc Natl Acad Sci U S A. 2011 Apr 26;108(17):6823-7. doi: 10.1073/pnas.1018191108. Epub 2011 Apr 11. Proc Natl Acad Sci U S A. 2011. PMID: 21482808 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources