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PMID: 2059621 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Determination of kinetic constants for peptidyl prolyl cis-trans isomerases by an improved spectrophotometric assay.

Biochemistry ·Vol. 30 ·No. 25 ·1991-06-25 ·Pages 6127-34

Kofron JL, Kuzmic P, Kishore V, Colón-Bonilla E, Rich DH

Abstract

The kinetic properties and substrate specificity of two well-characterized peptidyl prolyl cis-trans isomerases (PPIases), cyclophilin and the FK-506 binding protein (FKBP), have been previously examined [Fischer, G., Bang, H., Berger, E., & Schellenberger, A. (1984) Biochim. Biophys. Acta 791, 87-97; Harrison, R.K., & Stein, R.L. (1990) Biochemistry 29, 1684-1689; Albers, M.W., Walsh, C.T., & Schreiber, S. L. (1990) J. Org. Chem. 55, 4984-4986]. The chymotrypsin-coupled enzymatic assay employed in these studies suffers from two serious shortcomings. Due to the low equilibrium population of the X-cis-Pro-Phe-pNA isomer (the PPIase substrate), in conjunction with the low solubility of p-nitroaniline generated by chymotrypsin hydrolysis, substrate concentrations in the saturating region are not experimentally attainable. Secondly, the uncatalyzed cis-trans isomerization obscures the interpretation of the initial velocity. As a result of these limitations, the steady-state kinetic parameters (Km,Kcat) have not been determined. Here we introduce an improved version of the spectrophotometric assay and report for the first time the Michaelis constants and turnover numbers for both PPIases with established substrates. The improvements in the experimental conditions originate in a medium-induced increase in the equilibrium population of the cis X-Pro conformer and in conducting the assay at 0 degrees C to suppress the uncatalyzed thermal isomerization. In addition, we present a rigorous mathematical model of the spectrophotometric progress curves that accounts for the contributions of the residual background rate.(ABSTRACT TRUNCATED AT 250 WORDS)

MeSH Terms
Amino Acid Isomerases/antagonists & inhibitors,metabolism Aniline Compounds/pharmacology Animals Binding Sites Binding, Competitive Carrier Proteins/antagonists & inhibitors,metabolism Cattle Chymotrypsin/pharmacology Cyclosporins/pharmacology Humans Hydrolysis Kinetics Peptidylprolyl Isomerase Spectrophotometry Stereoisomerism Substrate Specificity/drug effects Thymus Gland/enzymology
Chemicals
Aniline Compounds Carrier Proteins Cyclosporins nitroaniline Chymotrypsin Amino Acid Isomerases Peptidylprolyl Isomerase
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Kofron J L
School of Pharmacy, University of Wisconsin, Madison 53706.
Kuzmic P
Kishore V
Colón-Bonilla E
Rich D H
Article Info
Journal
Biochemistry
Abbr.
Biochemistry
ISSN
0006-2960
Published
1991-06-25
Pages
6127-34
Language
English
Region
United States
NLM ID
0370623
Subset
IM
Grants
NIAID NIH HHS · AI24650 · United States
NIAMS NIH HHS · AR32007 · United States
Corrections
ErratumIn
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