Src is the kinase of the Helicobacter pylori CagA protein in vitro and in vivo

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Item Type:	Article
Title:	Src is the kinase of the Helicobacter pylori CagA protein in vitro and in vivo
Creators Name:	Selbach, M., Moese, S., Hauck, C.R., Meyer, T.F. and Backert, S.
Abstract:	The gastric pathogen Helicobacter pylori uses a type IV secretion system to inject the bacterial CagA protein into gastric epithelial cells. Within the host cell, CagA becomes phosphorylated on tyrosine residues and initiates cytoskeletal rearrangements. We demonstrate here that Src-like protein-tyrosine kinases mediate CagA phosphorylation in vitro and in vivo. First, the Src-specific tyrosine kinase inhibitor PP2 specifically blocks CagA phosphorylation and cytoskeletal rearrangements thereby inhibiting the CagA-induced hummingbird phenotype of gastric epithelial cells. Second, CagA is in vivo phosphorylated by transiently expressed c-Src. Third, recombinant c-Src and lysates derived from c-Src-expressing fibroblasts but not lysates derived from Src-, Yes-, and Fyn-deficient cells phosphorylated CagA in vitro. Fourth, a transfected CagA-GFP fusion protein is phosphorylated in vivo in Src-positive fibroblasts but not in Src-, Yes-, and Fyn-deficient cells. Because a CagA-GFP fusion protein mutated in an EPIYA motif is not efficiently phosphorylated in any of these fibroblast cells, the CagA EPIYA motif appears to constitute the major c-Src phosphorylation site conserved among CagA-positive Helicobacter strains.
Keywords:	3T3 Cells, Amino Acid Motifs, Amino Acid Sequence, Bacterial Antigens, Bacterial Proteins, Binding Sites, Cultured Cells, Cytoskeleton, Enzyme Inhibitors, Escherichia Coli, Fibroblasts, Green Fluorescent Proteins, Helicobacter Pylori, Luminescent Proteins, Molecular Sequence Data, Phenotype, Phosphorylation, Protein Binding, Proto-Oncogene Proteins, Proto-Oncogene Proteins c-fyn, Proto-Oncogene Proteins c-yes, Proto-Oncogene Proteins pp60(c-src), Recombinant Fusion Proteins, Recombinant Proteins, Transfection, src-Family Kinases, Animals, Mice
Source:	Journal of Biological Chemistry
ISSN:	0021-9258
Publisher:	American Society for Biochemistry and Molecular Biology
Volume:	277
Number:	9
Page Range:	6775-6778
Date:	1 March 2002
Official Publication:	https://doi.org/10.1074/jbc.C100754200
PubMed:	View item in PubMed

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