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PMID: 2479412 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Effect of chemically well-defined sphingosine and its N-methyl derivatives on protein kinase C and src kinase activities.

Biochemistry ·Vol. 28 ·No. 17 ·1989-08-22 ·Pages 6796-800

Igarashi Y, Hakomori S, Toyokuni T, Dean B, Fujita S, Sugimoto M, Ogawa T, el-Ghendy K, Racker E

Abstract

In view of the possible effects of the sphingoid base on protein kinases, and the fact that the sphingoid bases used in previous studies were not chemically well-defined, we have studied the effects of chemically well-defined sphingosines and their derivatives on kinase activity. Both (4E)-D- and (4E)-L-erythro-sphingenine showed a weak inhibitory effect, and (4E)-L-threo-sphingenine had a moderate inhibitory effect. In contrast, (4E)-N,N-dimethyl-D-erythro-sphingenine and the sphingosine preparation from a commercial source showed a strong inhibitory effect on PK-C in A431 cells as well as on purified PK-C. Synthetic (4E)-D-erythro-sphingenine and several samples of natural sphingosine inhibited v-src or c-src tyrosine kinase activity measured with polyglutamate-tyrosine (4:1) as substrate. N-Acetylated or N-methylated sphingosines did not inhibit src kinase activity, but rather produced a consistent 1.5-2-fold stimulation of such activity.

MeSH Terms
Animals Brain/enzymology Cell Line Humans Isomerism Kinetics Liposomes Protein Kinase C/metabolism Protein Kinases/metabolism Proto-Oncogene Proteins/metabolism Proto-Oncogene Proteins pp60(c-src) Rabbits Sphingosine/analogs & derivatives,chemical synthesis,pharmacology
Chemicals
Liposomes Proto-Oncogene Proteins Protein Kinases Proto-Oncogene Proteins pp60(c-src) Protein Kinase C Sphingosine
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Igarashi Y
Biomembrane Institute, Seattle, Washington 98119.
Hakomori S
Toyokuni T
Dean B
Fujita S
Sugimoto M
Ogawa T
el-Ghendy K
Racker E
Article Info
Journal
Biochemistry
Abbr.
Biochemistry
ISSN
0006-2960
Published
1989-08-22
Pages
6796-800
Language
English
Region
United States
NLM ID
0370623
Subset
IM
Grants
NCI NIH HHS · CA08964 · United States
NCI NIH HHS · CA42505 · United States
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