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PMID: 2271522 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Protein kinase C interaction with calcium: a phospholipid-dependent process.

Biochemistry ·Vol. 29 ·No. 33 ·1990-08-21 ·Pages 7624-30

Bazzi MD, Nelsestuen GL

Abstract

The calcium-binding properties of calcium- and phospholipid-dependent protein kinase C (PKC) were investigated by equilibrium dialysis in the presence and the absence of phospholipids. Calcium binding to PKC displayed striking and unexpected behavior; the free proteins bound virtually no calcium at intracellular calcium concentrations and bound limited calcium (about 1 mol/mol of PKC) at 200 microM calcium. However, in the presence of membranes containing acidic phospholipids, PKC bound at least eight calcium ions per protein. The presence of 1 microM phorbol dibutyrate (PDBu) in the dialysis buffer had little effect on these calcium-binding properties. Analysis of PKC-calcium binding by gel filtration under equilibrium conditions gave similar results; only membrane-associated PKC bound significant amounts of calcium. Consequently, PKC is a member of what may be a large group of proteins that bind calcium in a phospholipid-dependent manner. The calcium concentrations needed to induce PKC-membrane binding were similar to those needed for calcium binding (about 40 microM calcium at the midpoint). However, the calcium concentration required for PKC-membrane binding was strongly influenced by the phosphatidylserine composition of the membranes. Membranes with higher percentages of phosphatidylserine required lower concentrations of calcium. These properties suggested that the calcium sites may be generated at the interface between PKC and the membrane. Calcium may function as a bridge between PKC and phospholipids. These studies also suggested that calcium-dependent PKC-membrane binding and PKC function could be regulated by a number of factors in addition to calcium levels and diacylglycerol content of the membrane.

MeSH Terms
Calcium/metabolism Cell Membrane/drug effects,metabolism Dialysis Phorbol Esters/pharmacology Phospholipids/metabolism Protein Kinase C/metabolism
Chemicals
Phorbol Esters Phospholipids Protein Kinase C Calcium
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Bazzi M D
Department of Biochemistry, University of Minnesota, St. Paul 55108.
Nelsestuen G L
Article Info
Journal
Biochemistry
Abbr.
Biochemistry
ISSN
0006-2960
Published
1990-08-21
Pages
7624-30
Language
English
Region
United States
NLM ID
0370623
Subset
IM
Grants
NIGMS NIH HHS · GM 38819 · United States
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