Rapid Assay of Binding of Tumor-promoting Phorbol Esters to Protein Kinase C1
Overview
Authors
Affiliations
Protein kinase C is generally accepted to be a receptor protein of tumor-promoting phorbol esters. The binding of [3H]phorbol-12,13-dibutyrate to protein kinase C can be assayed by a rapid filtration procedure using a glass-fiber filter that has been treated with a cationic polymer, polyethylenimine. The phorbol ester specifically binds to the protein kinase only in the presence of phosphatidylserine and calcium. Non-specific binding is less than 10%, at most, of the total binding. The binding is linear with respect to the concentration of protein kinase C, is dependent on the concentrations of phorbol ester and phosphatidylserine in a saturative manner, and is inhibited by diacylglycerol (an endogenous activator of the protein kinase).
Corbalan-Garcia S, Gomez-Fernandez J Biophys Rev. 2017; 6(1):3-14.
PMID: 28509956 PMC: 5427809. DOI: 10.1007/s12551-013-0125-z.
Human deoxyhypusine synthase: interrelationship between binding of NAD and substrates.
Lee C, Park M Biochem J. 2000; 352 Pt 3:851-7.
PMID: 11104695 PMC: 1221526.
Wender P, DeBrabander J, Harran P, Jimenez J, Koehler M, Lippa B Proc Natl Acad Sci U S A. 1998; 95(12):6624-9.
PMID: 9618462 PMC: 22576. DOI: 10.1073/pnas.95.12.6624.
In vitro stimulation of protein kinase C by melatonin.
ANTON-TAY F, Ramirez G, Martinez I, Benitez-King G Neurochem Res. 1998; 23(5):601-6.
PMID: 9566597 DOI: 10.1023/a:1022474402458.
La Porta C, Comolli R Clin Exp Metastasis. 1997; 15(6):568-79.
PMID: 9344041 DOI: 10.1023/a:1018447531813.