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PMID: 3978106 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Action of phospholipase A2 on bilayers. Effect of inhibitors.

Biochimica et biophysica acta ·Vol. 814 ·No. 2 ·1985-04-11 ·Pages 319-26

Jain MK, Jahagirdar DV

Abstract

Action of several solutes on the kinetics of phospholipase-A2-catalyzed hydrolysis of the ternary codispersions containing dimyristoylphosphatidylcholine + 1-palmitoyllysophosphatidylcholine + palmitic acid is examined. The kinetics of hydrolysis is interpreted in terms of the ability of the enzyme to bind to the substrate interface. The inhibitory effect of these solutes is correlated with their ability to modify fluorescence intensity of the bound enzyme, to modify the phase-transition profile, and to inhibit aggregation/fusion of the ternary codispersions. Based on these observations, it is suggested that the solutes like n-alkanols, ketamine, alphadolone, alphaxalone, flufenamic acid, tobramycin, mepacrine, EMD 21657 and U-10029A modulate the phase equilibria in the codispersions and thus noncompetitively inhibit the phospholipase action. Inhibition by feverfew extract (Tanacetum parthemium) is also by a similar mechanism. Lipid-soluble drugs as indomethacin had little effect on the kinetics of hydrolysis. All these inhibitors decrease the total extent of hydrolysis of the available substrate. However, none of these inhibitors have any effect on the hydrolysis of monomeric substrate or on the inactivation of the phospholipase A2 by p-bromophenacylbromide. These observations suggest that all these inhibitors do not interact directly with the catalytic site of the free or the bound enzyme, and their effect is primarily on the enzyme-binding sites on the substrate vesicle, that is, by perturbation of lipid-protein interaction.

MeSH Terms
1-Octanol Animals Hexanols/pharmacology Hydrolysis Kinetics Lipid Bilayers/metabolism Octanols/pharmacology Pancreas/enzymology Phospholipases/metabolism Phospholipases A/antagonists & inhibitors,metabolism Phospholipases A2 Plants, Medicinal Propanolamines/pharmacology Sesquiterpenes/pharmacology Solutions Swine Tanacetum parthenium
Chemicals
Hexanols Lipid Bilayers Octanols Propanolamines Sesquiterpenes Solutions 1-hexanol U 10029A Phospholipases Phospholipases A Phospholipases A2 1-Octanol
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Jain M K
Jahagirdar D V
Article Info
Journal
Biochimica et biophysica acta
Abbr.
Biochim Biophys Acta
ISSN
0006-3002
Published
1985-04-11
Pages
319-26
Language
English
Region
Netherlands
NLM ID
0217513
Subset
IM
Grants
NIGMS NIH HHS · PHS-GM 29703 · United States
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