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PMID: 10985781 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

The C1 and C2 domains of protein kinase C are independent membrane targeting modules, with specificity for phosphatidylserine conferred by the C1 domain.

Biochemistry ·Vol. 39 ·No. 37 ·2000-09-19 ·Pages 11360-9

Johnson JE, Giorgione J, Newton AC

Abstract

Protein kinase C is specifically activated by binding two membrane lipids: the second messenger, diacylglycerol, and the amino phospholipid, phosphatidylserine. This binding provides the energy to release an autoinhibitory pseudosubstrate from the active site. Interaction with these lipids recruits the enzyme to the membrane by engaging two membrane-targeting modules: the C1 domain (present as a tandem repeat in most protein kinase Cs) and the C2 domain. Here we dissect the contribution of each domain in recruiting protein kinase C betaII to membranes. Binding analyses of recombinant domains reveal that the C2 domain binds anionic lipids in a Ca(2+)-dependent, but diacylglycerol-independent, manner, with little selectivity for phospholipid headgroup beyond the requirement for negative charge. The C1B domain binds membranes in a diacylglycerol/phorbol ester-dependent, but Ca(2+)-independent manner. Like the C2 domain, the C1B domain preferentially binds anionic lipids. However, in striking contrast to the C2 domain, the C1B domain binds phosphatidylserine with an order of magnitude higher affinity than other anionic lipids. This preference for phosphatidylserine is, like that of the full-length protein, stereoselective for sn-1, 2-phosphatidyl-L-serine. Quantitative analysis of binding constants of individual domains and that of full-length protein reveals that the full-length protein binds membranes with lower affinity than expected based on the binding affinity of isolated domains. In addition to entropic and steric considerations, the difference in binding energy may reflect the energy required to expel the pseudosubstrate from the substrate binding cavity. This study establishes that each module is an independent membrane-targeting module with each, independently of the other, containing determinants for membrane recognition. The presence of each of these modules, separately, in a number of other signaling proteins epitomizes the use of these modules as discreet membrane targets.

MeSH Terms
Calcium/chemistry Diglycerides/pharmacology Enzyme Activation/drug effects,genetics Escherichia coli/genetics Genetic Vectors/chemical synthesis Lipid Bilayers/chemistry,metabolism Peptide Fragments/chemistry,genetics,metabolism Phosphatidylserines/chemistry,metabolism Protein Binding/drug effects,genetics Protein Kinase C/chemistry,genetics,metabolism Protein Structure, Tertiary/drug effects,genetics Substrate Specificity/drug effects,genetics Tetradecanoylphorbol Acetate/pharmacology
Chemicals
Diglycerides Lipid Bilayers Peptide Fragments Phosphatidylserines Protein Kinase C Tetradecanoylphorbol Acetate Calcium
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Johnson J E
Department of Pharmacology, University of California at San Diego, La Jolla, California 92093-0640, USA.
Giorgione J
Newton A C
Article Info
Journal
Biochemistry
Abbr.
Biochemistry
ISSN
0006-2960
Published
2000-09-19
Pages
11360-9
Language
English
Region
United States
NLM ID
0370623
Subset
IM
Grants
NIGMS NIH HHS · GM 43154 · United States
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