Identification of a novel protein complex containing annexin VI, Fyn, Pyk2, and the p120(GAP) C2 domain
p120(GAP) (RasGAP) has been proposed to function as both an inhibitor and effector of Ras. Previously we have shown that RasGAP contains a C2 domain which mediates both Ca(2+)-dependent membrane association and protein-protein interactions. Specifically, three proteins have been isolated in a comple...
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Veröffentlicht in: | FEBS letters 2000-03, Vol.469 (1), p.88-92 |
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description | p120(GAP) (RasGAP) has been proposed to function as both an inhibitor and effector of Ras. Previously we have shown that RasGAP contains a C2 domain which mediates both Ca(2+)-dependent membrane association and protein-protein interactions. Specifically, three proteins have been isolated in a complex with the C2 domain of RasGAP; these are the Ca(2+)-dependent lipid binding protein annexin VI (p70) and two previously unidentified proteins, p55 and p120. Here we provide evidence that p55 is the Src family kinase Fyn and p120 is the focal adhesion kinase family member Pyk2. In addition, in vitro binding assays indicate that Fyn, but not Pyk2 binds directly to annexin VI. Finally, co-immunoprecipitation studies in Rat-1 fibroblasts confirm that Fyn, Pyk2, annexin VI and RasGAP can form a protein complex in mammalian cells. |
doi_str_mv | 10.1016/S0014-5793(00)01252-7 |
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Previously we have shown that RasGAP contains a C2 domain which mediates both Ca(2+)-dependent membrane association and protein-protein interactions. Specifically, three proteins have been isolated in a complex with the C2 domain of RasGAP; these are the Ca(2+)-dependent lipid binding protein annexin VI (p70) and two previously unidentified proteins, p55 and p120. Here we provide evidence that p55 is the Src family kinase Fyn and p120 is the focal adhesion kinase family member Pyk2. In addition, in vitro binding assays indicate that Fyn, but not Pyk2 binds directly to annexin VI. Finally, co-immunoprecipitation studies in Rat-1 fibroblasts confirm that Fyn, Pyk2, annexin VI and RasGAP can form a protein complex in mammalian cells.</description><identifier>ISSN: 0014-5793</identifier><identifier>DOI: 10.1016/S0014-5793(00)01252-7</identifier><identifier>PMID: 10708762</identifier><language>eng</language><publisher>England</publisher><subject>Animals ; Annexin A6 - metabolism ; Cells, Cultured ; Focal Adhesion Kinase 2 ; Multienzyme Complexes - chemistry ; Multienzyme Complexes - metabolism ; p120 GTPase Activating Protein - metabolism ; Precipitin Tests ; Protein Binding ; Protein-Tyrosine Kinases - metabolism ; Proto-Oncogene Proteins - metabolism ; Proto-Oncogene Proteins c-fyn ; Rats ; Sheep ; Signal Transduction ; Transfection</subject><ispartof>FEBS letters, 2000-03, Vol.469 (1), p.88-92</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c284t-792add7f39f35a889974a3f35c75b794e3df5e35fbb040fe654956ddfb85c3813</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10708762$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chow, A</creatorcontrib><creatorcontrib>Davis, A J</creatorcontrib><creatorcontrib>Gawler, D J</creatorcontrib><title>Identification of a novel protein complex containing annexin VI, Fyn, Pyk2, and the p120(GAP) C2 domain</title><title>FEBS letters</title><addtitle>FEBS Lett</addtitle><description>p120(GAP) (RasGAP) has been proposed to function as both an inhibitor and effector of Ras. 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Finally, co-immunoprecipitation studies in Rat-1 fibroblasts confirm that Fyn, Pyk2, annexin VI and RasGAP can form a protein complex in mammalian cells.</description><subject>Animals</subject><subject>Annexin A6 - metabolism</subject><subject>Cells, Cultured</subject><subject>Focal Adhesion Kinase 2</subject><subject>Multienzyme Complexes - chemistry</subject><subject>Multienzyme Complexes - metabolism</subject><subject>p120 GTPase Activating Protein - metabolism</subject><subject>Precipitin Tests</subject><subject>Protein Binding</subject><subject>Protein-Tyrosine Kinases - metabolism</subject><subject>Proto-Oncogene Proteins - metabolism</subject><subject>Proto-Oncogene Proteins c-fyn</subject><subject>Rats</subject><subject>Sheep</subject><subject>Signal Transduction</subject><subject>Transfection</subject><issn>0014-5793</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9UE1LAzEUzEGxtfoTlJzEQlfzsdkkx1JsLRQs-HFdspukRneTtZtK--8NWD3NvHkzw-MBcIXRHUa4uH9GCOcZ45LeIjRGmDCS8RMw_JcH4LzvP1CaBZZnYIARR4IXZAg2S218dNbVKrrgYbBQQR--TQO7bYjGeViHtmvMPqGPynnnN1B5b_Zp9bacwPnBT-D68EkmSdYwvhvYYYJuF9P1GM4I1KFNqQtwalXTm8sjjsDr_OFl9pitnhbL2XSV1UTkMeOSKK25pdJSpoSQkueKJl5zVnGZG6otM5TZqkI5sqZguWSF1rYSrKYC0xG4-e1N13_tTB_L1vW1aRrlTdj1JUeS5ZSIZLw-GndVa3TZbV2rtofy7zX0B7M4Ysw</recordid><startdate>20000303</startdate><enddate>20000303</enddate><creator>Chow, A</creator><creator>Davis, A J</creator><creator>Gawler, D J</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20000303</creationdate><title>Identification of a novel protein complex containing annexin VI, Fyn, Pyk2, and the p120(GAP) C2 domain</title><author>Chow, A ; Davis, A J ; Gawler, D J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c284t-792add7f39f35a889974a3f35c75b794e3df5e35fbb040fe654956ddfb85c3813</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Animals</topic><topic>Annexin A6 - metabolism</topic><topic>Cells, Cultured</topic><topic>Focal Adhesion Kinase 2</topic><topic>Multienzyme Complexes - chemistry</topic><topic>Multienzyme Complexes - metabolism</topic><topic>p120 GTPase Activating Protein - metabolism</topic><topic>Precipitin Tests</topic><topic>Protein Binding</topic><topic>Protein-Tyrosine Kinases - metabolism</topic><topic>Proto-Oncogene Proteins - metabolism</topic><topic>Proto-Oncogene Proteins c-fyn</topic><topic>Rats</topic><topic>Sheep</topic><topic>Signal Transduction</topic><topic>Transfection</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chow, A</creatorcontrib><creatorcontrib>Davis, A J</creatorcontrib><creatorcontrib>Gawler, D J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>FEBS letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chow, A</au><au>Davis, A J</au><au>Gawler, D J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of a novel protein complex containing annexin VI, Fyn, Pyk2, and the p120(GAP) C2 domain</atitle><jtitle>FEBS letters</jtitle><addtitle>FEBS Lett</addtitle><date>2000-03-03</date><risdate>2000</risdate><volume>469</volume><issue>1</issue><spage>88</spage><epage>92</epage><pages>88-92</pages><issn>0014-5793</issn><abstract>p120(GAP) (RasGAP) has been proposed to function as both an inhibitor and effector of Ras. Previously we have shown that RasGAP contains a C2 domain which mediates both Ca(2+)-dependent membrane association and protein-protein interactions. Specifically, three proteins have been isolated in a complex with the C2 domain of RasGAP; these are the Ca(2+)-dependent lipid binding protein annexin VI (p70) and two previously unidentified proteins, p55 and p120. Here we provide evidence that p55 is the Src family kinase Fyn and p120 is the focal adhesion kinase family member Pyk2. In addition, in vitro binding assays indicate that Fyn, but not Pyk2 binds directly to annexin VI. Finally, co-immunoprecipitation studies in Rat-1 fibroblasts confirm that Fyn, Pyk2, annexin VI and RasGAP can form a protein complex in mammalian cells.</abstract><cop>England</cop><pmid>10708762</pmid><doi>10.1016/S0014-5793(00)01252-7</doi><tpages>5</tpages></addata></record> |
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subjects | Animals Annexin A6 - metabolism Cells, Cultured Focal Adhesion Kinase 2 Multienzyme Complexes - chemistry Multienzyme Complexes - metabolism p120 GTPase Activating Protein - metabolism Precipitin Tests Protein Binding Protein-Tyrosine Kinases - metabolism Proto-Oncogene Proteins - metabolism Proto-Oncogene Proteins c-fyn Rats Sheep Signal Transduction Transfection |
title | Identification of a novel protein complex containing annexin VI, Fyn, Pyk2, and the p120(GAP) C2 domain |
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