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PMID: 2530215 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Cyclopiazonic acid is a specific inhibitor of the Ca2+-ATPase of sarcoplasmic reticulum.

The Journal of biological chemistry ·Vol. 264 ·No. 30 ·1989-10-25 ·Pages 17816-23

Seidler NW, Jona I, Vegh M, Martonosi A

Abstract

The mycotoxin, cyclopiazonic acid (CPA), inhibits the Ca2+-stimulated ATPase (EC 3.6.1.38) and Ca2+ transport activity of sarcoplasmic reticulum (Goeger, D. E., Riley, R. T., Dorner, J. W., and Cole, R. J. (1988) Biochem. Pharmacol. 37, 978-981). We found that at low ATP concentrations (0.5-2 microM) the inhibition of ATPase activity was essentially complete at a CPA concentration of 6-8 nmol/mg protein, indicating stoichiometric reaction of CPA with the Ca2+-ATPase. Cyclopiazonic acid caused similar inhibition of the Ca2+-stimulated ATP hydrolysis in intact sarcoplasmic reticulum and in a purified preparation of Ca2+-ATPase. Cyclopiazonic acid also inhibited the Ca2+-dependent acetylphosphate, p-nitrophenylphosphate and carbamylphosphate hydrolysis by sarcoplasmic reticulum. ATP protected the enzyme in a competitive manner against inhibition by CPA, while a 10(5)-fold change in free Ca2+ concentration had only moderate effect on the extent of inhibition. CPA did not influence the crystallization of Ca2+-ATPase by vanadate or the reaction of fluorescein-5'-isothiocyanate with the Ca2+-ATPase, but it completely blocked at concentrations as low as 1-2 mol of CPA/mol of ATPase the fluorescence changes induced by Ca2+ and [ethylenebis(oxyethylenenitrilo)]tetraacetic acid (EGTA) in FITC-labeled sarcoplasmic reticulum and inhibited the cleavage of Ca2+-ATPase by trypsin at the T2 cleavage site in the presence of EGTA. These observations suggest that CPA interferes with the ATP-induced conformational changes related to Ca2+ transport. The effect of CPA on the sarcoplasmic reticulum Ca2+-ATPase appears to be fairly specific, since the kidney and brain Na+,K+-ATPase (EC 3.6.1.37), the gastric H+,K+-ATPase (EC 3.6.1.36), the mitochondrial F1-ATPase (EC 3.6.1.34), the Ca2+-ATPase of erythrocytes, and the Mg2+-activated ATPase of T-tubules and surface membranes of rat skeletal muscle were not inhibited by CPA, even at concentrations as high as 1000 nmol/mg protein.

MeSH Terms
Adenosine Triphosphatases/isolation & purification,metabolism Animals Calcium-Transporting ATPases/antagonists & inhibitors,isolation & purification Cattle Cell Membrane/enzymology Erythrocyte Membrane/enzymology Gastric Mucosa/enzymology Indoles/pharmacology Kinetics Mitochondria, Heart/enzymology Muscles/enzymology Mycotoxins/pharmacology Peptide Fragments/isolation & purification Proton-Translocating ATPases/metabolism Rabbits Sarcoplasmic Reticulum/enzymology Swine Trypsin/metabolism
Chemicals
Indoles Mycotoxins Peptide Fragments Trypsin Adenosine Triphosphatases Proton-Translocating ATPases Calcium-Transporting ATPases cyclopiazonic acid
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Seidler N W
Department of Biochemistry and Molecular Biology, State University of New York Health Science Center, Syracuse 13210.
Jona I
Vegh M
Martonosi A
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1989-10-25
Pages
17816-23
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NIAMS NIH HHS · AR 26645 · United States
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