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PMID: 8387502 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Regulation of purified subtypes of phosphatidylinositol-specific phospholipase C beta by G protein alpha and beta gamma subunits.

The Journal of biological chemistry ·Vol. 268 ·No. 13 ·1993-05-05 ·Pages 9667-74

Smrcka AV, Sternweis PC

Abstract

Specific antisera were produced to peptides representing the carboxyl termini of three subtypes of phosphatidylinositol-specific phospholipase C (PIPLC) beta which have been identified by isolation of cDNAs (Kriz, R., Lin, L., Sultzman, L., Ellis, C., Heldin, C., Pawson, T., and Knopf, J. (1990) Ciba Found. Symp. 150, 112-127). Screening with the antisera indicates that PIPLC beta 3 is present in a variety of cell lines and rat tissues, whereas the distribution of PIPLC beta 1 and beta 2 is more restricted. A combination of conventional and immunoaffinity chromatographic techniques was used to purify PIPLC beta 1 and beta 3 from rat brain membranes. PIPLC beta 2 was purified from cytosol of HL60 cells. All three subtypes were activated by purified G protein alpha q/11 subunits with the following relative efficacies: PIPLC beta 3 > or = PIPLC beta 1 >> PIPLC beta 2. All three PIPLC subtypes were also activated by G protein beta gamma subunits with varying efficacies. The presence of beta gamma subunits depressed the ability of alpha q/11 to activate PIPLC beta 1 and beta 3 at low Mg2+ concentrations (1 mM). At higher concentrations of Mg2+ (2 mM or greater), activation of PIPLC beta 3, but not PIPLC beta 1, by beta gamma and alpha q/11 became additive. PIPLC beta 3 was activated by alpha q/11 even in the presence of a saturating concentration of beta gamma subunits. This indicates that there are separate sites for interaction of PIPLCs with G protein subunits and that this interaction differs depending on the enzyme subtype and the concentration of Mg2+.

MeSH Terms
Amino Acid Sequence Animals Brain/enzymology Cell Membrane/enzymology Chromatography, Affinity Enzyme Activation GTP-Binding Proteins/metabolism Humans Immunoglobulin G Isoenzymes/metabolism Kinetics Leukemia, Promyelocytic, Acute Macromolecular Substances Magnesium Chloride/pharmacology Models, Biological Molecular Sequence Data Peptide Fragments/isolation & purification Phosphatidylinositol Diacylglycerol-Lyase Phosphoinositide Phospholipase C Phosphoric Diester Hydrolases/metabolism Rats Tumor Cells, Cultured
Chemicals
Immunoglobulin G Isoenzymes Macromolecular Substances Peptide Fragments Magnesium Chloride Phosphoric Diester Hydrolases Phosphoinositide Phospholipase C GTP-Binding Proteins Phosphatidylinositol Diacylglycerol-Lyase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Smrcka A V
Department of Pharmacology, Southwestern Graduate School of Biomedical Science, University of Texas Southwestern Medical Center, Dallas 75235-9041.
Sternweis P C
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1993-05-05
Pages
9667-74
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NIGMS NIH HHS · R01-GM31954 · United States
NIGMS NIH HHS · S32-GM14489 · United States
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