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PMID: 6298006 Published · ppublish English Comparative Study Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Cobra polypeptide cytotoxin I and marine worm polypeptide cytotoxin A-IV are potent and selective inhibitors of phospholipid-sensitive Ca2+-dependent protein kinase.

FEBS letters ·Vol. 153 ·No. 1 ·1983-03-07 ·Pages 183-6

Kuo JF, Raynor RL, Mazzei GJ, Schatzman RC, Turner RS, Kem WR

Abstract

The effects of a number of polypeptide cytotoxins and neurotoxins on various protein kinases were examined. It was found that cobra cytotoxin I and marine worm cytotoxin A-IV effectively and specifically inhibited phospholipid-sensitive Ca2+-dependent protein kinase (PL-Ca-PK) relative to myosin light chain kinase and cyclic nucleotide-dependent protein kinases. Inhibition of PL-Ca-PK by these cytotoxins could be overcome by phosphatidylserine. Neurotoxins, in comparison, were much less effective inhibitors. The present findings indicated that these polypeptide cytotoxins, unlike other agents reported to date, were selective inhibitors of PL-Ca-PK and could be used to differentiate Ca2+-dependent events regulated by phospholipid or calmodulin.

MeSH Terms
Bee Venoms/pharmacology Calcium/pharmacology Cobra Neurotoxin Proteins/pharmacology Cyclic AMP/pharmacology Cyclic GMP/pharmacology Cytotoxins/pharmacology Elapid Venoms/pharmacology Kinetics Marine Toxins/pharmacology Myosin-Light-Chain Kinase Phosphatidylserines/pharmacology Phospholipids/pharmacology Protein Kinase Inhibitors
Chemicals
Bee Venoms Cerebratulus lacteus toxin A-IV Cobra Neurotoxin Proteins Cytotoxins Elapid Venoms Marine Toxins Phosphatidylserines Phospholipids Protein Kinase Inhibitors cobra cytotoxin I Cyclic AMP Myosin-Light-Chain Kinase Cyclic GMP Calcium
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Kuo J F
Raynor R L
Mazzei G J
Schatzman R C
Turner R S
Kem W R
Article Info
Journal
FEBS letters
Abbr.
FEBS Lett
ISSN
0014-5793
Published
1983-03-07
Pages
183-6
Language
English
Region
England
NLM ID
0155157
Subset
IM
Grants
NIGMS NIH HHS · GM-25849 · United States
NHLBI NIH HHS · HL-15696 · United States
NINDS NIH HHS · NS-17608 · United States
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