Abstract
The signaling subunits of antigen receptor and Fc receptor complexes carry a tyrosin-based activation motif (ITAM). Work of the recent years showed that this motif is required for the activation of protein tyrosine kinases (PTK) via these receptors. We discuss here two models of how ITAM either in its phosphorylated or unphosphorylated state may interact with PTKs. After receptor cross-linking the activated PTKs will also phosphorylate the tyrosines of ITAM. We have found that different members of the src-family of kinases can phosphorylate either both tyrosines or only the first tyrosine of ITAM. We further discuss how this alternative phosphorylation of ITAM can result in the interaction of the BCR with different SH2-containing proteins and thus influence the signal transduction from the receptor.
Publication types
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Research Support, Non-U.S. Gov't
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Review
MeSH terms
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Amino Acid Sequence
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Antigens, CD / metabolism*
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CD79 Antigens
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Enzyme Activation / immunology*
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Enzyme Precursors / immunology
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Enzyme Precursors / metabolism
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Intracellular Signaling Peptides and Proteins
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Models, Immunological
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Molecular Sequence Data
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Oncogene Protein pp60(v-src) / immunology
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Oncogene Protein pp60(v-src) / metabolism
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Protein-Tyrosine Kinases / immunology
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Protein-Tyrosine Kinases / metabolism*
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Receptors, Antigen, B-Cell / immunology
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Receptors, Antigen, B-Cell / metabolism*
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Receptors, Fc / immunology
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Receptors, Fc / metabolism
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Sequence Homology, Amino Acid
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Signal Transduction / immunology
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Syk Kinase
Substances
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Antigens, CD
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CD79 Antigens
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Enzyme Precursors
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Intracellular Signaling Peptides and Proteins
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Receptors, Antigen, B-Cell
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Receptors, Fc
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Protein-Tyrosine Kinases
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Oncogene Protein pp60(v-src)
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Syk Kinase