» Articles » PMID: 6298006

Cobra Polypeptide Cytotoxin I and Marine Worm Polypeptide Cytotoxin A-IV Are Potent and Selective Inhibitors of Phospholipid-sensitive Ca2+-dependent Protein Kinase

Overview
Journal FEBS Lett
Specialty Biochemistry
Date 1983 Mar 7
PMID 6298006
Citations 19
Authors
Affiliations
Soon will be listed here.
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.

Citing Articles

The Toxins of Nemertean Worms.

Goransson U, Jacobsson E, Strand M, Andersson H Toxins (Basel). 2019; 11(2).

PMID: 30781381 PMC: 6410017. DOI: 10.3390/toxins11020120.


Cancer cell injury by cytotoxins from cobra venom is mediated through lysosomal damage.

Feofanov A, Sharonov G, Astapova M, Rodionov D, Utkin Y, Arseniev A Biochem J. 2005; 390(Pt 1):11-8.

PMID: 15847607 PMC: 1184559. DOI: 10.1042/BJ20041892.


Protein kinase C involvement in maintenance and modulation of noradrenaline release in the mouse brain cortex.

Schroeder G, Kotsonis P, Musgrave I, Majewski H Br J Pharmacol. 1995; 116(6):2757-63.

PMID: 8591001 PMC: 1909115. DOI: 10.1111/j.1476-5381.1995.tb17238.x.


Field stimulation-induced noradrenaline release from guinea-pig atria is modulated by prejunctional alpha 2-adrenoceptors and protein kinase C.

Brasch H Basic Res Cardiol. 1993; 88(6):545-56.

PMID: 8147820 DOI: 10.1007/BF00788873.


Polyamines inhibit phospholipid-sensitive and calmodulin-sensitive Ca2+-dependent protein kinases.

Qi D, Schatzman R, Mazzei G, Turner R, Raynor R, Liao S Biochem J. 1983; 213(2):281-8.

PMID: 6615435 PMC: 1152126. DOI: 10.1042/bj2130281.