Home LiteratureArticle Details
PMID: 8144564 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Identification, partial purification, and characterization of a novel phospholipid-dependent and fatty acid-activated protein kinase from human platelets.

The Journal of biological chemistry ·Vol. 269 ·No. 13 ·1994-04-01 ·Pages 9729-35

Khan WA, Blobe GC, Richards AL, Hannun YA

Abstract

A novel lipid-dependent protein kinase in human platelets was partially purified and characterized. This enzyme was calcium-independent and was selective for phosphatidic acid as a cofactor/activator with initial activation observed at approximately 2 mol % and peak activity achieved at 4 mol % phosphatidic acid. In the presence of phosphatidylserine, enzyme activation was observed with concentrations of phosphatidic acid as low as 0.5 mol % with peak activity at 2 mol %. Other anionic phospholipids also activated the enzyme but to a lesser extent and with less potency. Enzyme activity was independent of diacylglycerol or phorbol esters and the enzyme did not bind [3H]phorbol dibutyrate. In a soluble protein kinase assay, the enzyme was activated by cis-unsaturated fatty acids with maximum activation occurring at 5-10 microM sodium oleate. Western blot analysis showed that this enzyme did not cross-react immunologically with antibodies raised against the currently identified isoenzymes of protein kinase C. A number of additional biochemical criteria distinguished this enzyme from known isoenzymes of protein kinase C. These biochemical and immunologic data define a novel lipid-dependent protein kinase in human platelets. The role of this enzyme in signal transduction as a phosphatidic acid-activated enzyme and as a possible target for cis-unsaturated fatty acids is discussed.

MeSH Terms
1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine Blood Platelets/enzymology Blotting, Western Calcium/pharmacology Chromatography Chromatography, Affinity Chromatography, Ion Exchange Diglycerides/pharmacology Durapatite Enzyme Activation Humans Isoquinolines/pharmacology Kinetics Oleic Acid Oleic Acids/pharmacology Phorbol 12,13-Dibutyrate/metabolism Phospholipids/pharmacology Piperazines/pharmacology Protein Kinase Inhibitors Protein Kinases/blood,isolation & purification Sphingosine/pharmacology Substrate Specificity
Chemicals
Diglycerides Isoquinolines Oleic Acids Phospholipids Piperazines Protein Kinase Inhibitors Oleic Acid Phorbol 12,13-Dibutyrate 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine Durapatite Protein Kinases Sphingosine Calcium
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Khan W A
Department of Medicine, Duke University Medical Center, Durham, North Carolina 27710.
Blobe G C
Richards A L
Hannun Y A
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1994-04-01
Pages
9729-35
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NHLBI NIH HHS · HL43707 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com