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PMID: 11410586 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Activation loop Ser744 and Ser748 in protein kinase D are transphosphorylated in vivo.

The Journal of biological chemistry ·Vol. 276 ·No. 35 ·2001-08-31 ·Pages 32606-15

Waldron RT, Rey O, Iglesias T, Tugal T, Cantrell D, Rozengurt E

Abstract

The importance of activation loop phosphorylation in the regulation of protein kinase D (PKD/protein kinase C (PKC) mu) activity has become controversial. In order to clarify the mechanism(s) of PKD activation, we developed a novel phosphospecific antibody recognizing phosphorylated Ser(748) in PKD (pS748). Western blot analysis with the pS748 antibody, carried out with a variety of PKD forms and in a variety of cell types including full-length PKD transfected in COS-7 and HEK 293 cells, a green fluorescent protein-PKD fusion protein transfected in either Swiss 3T3 fibroblasts or Madin-Darby canine kidney epithelial cells, and endogenous PKD expressed in A20 lymphocytes and Rat-1 fibroblasts, indicated that Ser(748) phosphorylation was absent from unstimulated cells. In contrast, dramatic increases in Ser(748) phosphorylation were induced by phorbol esters, bombesin, or cross-linking of B lymphocyte antigen receptors or by cotransfection with active PKCepsilon or PKCeta. Western analysis using a second phosphospecific antibody, which primarily recognizes PKD phosphorylated at Ser(744), revealed that Ser(744) phosphorylation accompanies Ser(748) phosphorylation during PKD activation in vivo. Ser(744)/Ser(748) phosphorylation requires PKC but not PKD activity, indicative of transphosphorylation. Our results provide new experimental evidence indicating that activation loop phosphorylation at Ser(744) and Ser(748) occurs during PKD activation in vivo and support the notion of a PKC-PKD phosphorylation cascade.

MeSH Terms
3T3 Cells Amino Acid Sequence Amino Acid Substitution Animals Antibodies COS Cells Cell Line Chlorocebus aethiops Enzyme Activation Green Fluorescent Proteins Humans Kinetics Luminescent Proteins/analysis Mice Molecular Sequence Data Mutagenesis, Site-Directed Peptide Fragments/chemistry,immunology Phosphorylation Protein Kinase C/chemistry,genetics,metabolism Rats Recombinant Fusion Proteins/analysis,metabolism Recombinant Proteins/chemistry,metabolism Serine Transfection
Chemicals
Antibodies Luminescent Proteins Peptide Fragments Recombinant Fusion Proteins Recombinant Proteins Green Fluorescent Proteins Serine protein kinase D Protein Kinase C
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Waldron R T
Unit of Signal Transduction and Gastrointestinal Cancer, Division of Digestive Diseases, Department of Medicine, and Molecular Biology Institute, UCLA School of Medicine and UCLA-CURE Digestive Diseases Research Center, Los Angeles, California 90095, USA.
Rey O
Iglesias T
Tugal T
Cantrell D
Rozengurt E
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2001-08-31
Epub
2001-00-15
Pages
32606-15
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NIDDK NIH HHS · DK17294 · United States
NIDDK NIH HHS · DK55003 · United States
NIDDK NIH HHS · DK55003-01S1 · United States
NIDDK NIH HHS · DK56930 · United States
NIDDK NIH HHS · K01 DK 02834-01 · United States
NCI NIH HHS · P50 CA90388-01 · United States
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