ADP Is the Cognate Ligand for the Orphan G Protein-coupled Receptor SP1999
P2Y receptors are a class of G protein-coupled receptors activated primarily by ATP, UTP, and UDP. Five mammalian P2Y receptors have been cloned so far including P2Y1, P2Y2, P2Y4, P2Y6, and P2Y11. P2Y1, P2Y2, and P2Y6 couple to the activation of phospholipase C, whereas P2Y4 and P2Y11 couple to the...
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Veröffentlicht in: | The Journal of biological chemistry 2001-03, Vol.276 (11), p.8608-8615 |
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container_title | The Journal of biological chemistry |
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creator | Zhang, Fang L. Luo, Lin Gustafson, Eric Lachowicz, Jean Smith, Michelle Qiao, Xudong Liu, Yan-Hui Chen, Guodong Pramanik, Birendra Laz, Thomas M. Palmer, Kyle Bayne, Marvin Monsma, Frederick J. |
description | P2Y receptors are a class of G protein-coupled receptors activated primarily by ATP, UTP, and UDP. Five mammalian P2Y receptors have been cloned so far including P2Y1, P2Y2, P2Y4, P2Y6, and P2Y11. P2Y1, P2Y2, and P2Y6 couple to the activation of phospholipase C, whereas P2Y4 and P2Y11 couple to the activation of both phospholipase C and the adenylyl cyclase pathways. Additional ADP receptors linked to Gαi have been described but have not yet been cloned. SP1999 is an orphan G protein-coupled receptor, which is highly expressed in brain, spinal cord, and blood platelets. In the present study, we demonstrate that SP1999 is a Gαi-coupled receptor that is potently activated by ADP. In an effort to identify ligands for SP1999, fractionated rat spinal cord extracts were assayed for Ca2+ mobilization activity against Chinese hamster ovary cells transiently transfected with SP1999 and chimeric Gα subunits (Gαq/i). A substance that selectively activated SP1999-transfected cells was identified and purified through a series of chromatographic steps. Mass spectral analysis of the purified material definitively identified it as ADP. ADP was subsequently shown to inhibit forskolin-stimulated adenylyl cyclase activity through selective activation of SP1999 with an EC50 of 60 nm. Other nucleotides were able to activate SP1999 with a rank order of potency 2-MeS-ATP = 2-MeS-ADP > ADP = adenosine 5′-O-2-(thio)diphosphate > 2-Cl-ATP > adenosine 5′-O-(thiotriphosphate). Thus, SP1999 is a novel, Gαi-linked receptor for ADP.AF321815 |
doi_str_mv | 10.1074/jbc.M009718200 |
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Five mammalian P2Y receptors have been cloned so far including P2Y1, P2Y2, P2Y4, P2Y6, and P2Y11. P2Y1, P2Y2, and P2Y6 couple to the activation of phospholipase C, whereas P2Y4 and P2Y11 couple to the activation of both phospholipase C and the adenylyl cyclase pathways. Additional ADP receptors linked to Gαi have been described but have not yet been cloned. SP1999 is an orphan G protein-coupled receptor, which is highly expressed in brain, spinal cord, and blood platelets. In the present study, we demonstrate that SP1999 is a Gαi-coupled receptor that is potently activated by ADP. In an effort to identify ligands for SP1999, fractionated rat spinal cord extracts were assayed for Ca2+ mobilization activity against Chinese hamster ovary cells transiently transfected with SP1999 and chimeric Gα subunits (Gαq/i). A substance that selectively activated SP1999-transfected cells was identified and purified through a series of chromatographic steps. Mass spectral analysis of the purified material definitively identified it as ADP. ADP was subsequently shown to inhibit forskolin-stimulated adenylyl cyclase activity through selective activation of SP1999 with an EC50 of 60 nm. Other nucleotides were able to activate SP1999 with a rank order of potency 2-MeS-ATP = 2-MeS-ADP > ADP = adenosine 5′-O-2-(thio)diphosphate > 2-Cl-ATP > adenosine 5′-O-(thiotriphosphate). Thus, SP1999 is a novel, Gαi-linked receptor for ADP.AF321815</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.M009718200</identifier><identifier>PMID: 11104774</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>3T3 Cells ; Adenosine Diphosphate - metabolism ; Amino Acid Sequence ; Animals ; Base Sequence ; CHO Cells ; Cloning, Molecular ; Cricetinae ; DNA, Complementary - chemistry ; Gene Expression Profiling ; GTP-Binding Proteins - metabolism ; Humans ; Ligands ; Mice ; Molecular Sequence Data ; Rats ; Receptors, Purinergic P2 - metabolism ; Receptors, Purinergic P2Y1</subject><ispartof>The Journal of biological chemistry, 2001-03, Vol.276 (11), p.8608-8615</ispartof><rights>2001 © 2001 ASBMB. Currently published by Elsevier Inc; originally published by American Society for Biochemistry and Molecular Biology.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-8e82c59edd1f445fd6362658d3d9a50622e9f806d59841732bd34e94edbd48543</citedby><cites>FETCH-LOGICAL-c474t-8e82c59edd1f445fd6362658d3d9a50622e9f806d59841732bd34e94edbd48543</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11104774$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Fang L.</creatorcontrib><creatorcontrib>Luo, Lin</creatorcontrib><creatorcontrib>Gustafson, Eric</creatorcontrib><creatorcontrib>Lachowicz, Jean</creatorcontrib><creatorcontrib>Smith, Michelle</creatorcontrib><creatorcontrib>Qiao, Xudong</creatorcontrib><creatorcontrib>Liu, Yan-Hui</creatorcontrib><creatorcontrib>Chen, Guodong</creatorcontrib><creatorcontrib>Pramanik, Birendra</creatorcontrib><creatorcontrib>Laz, Thomas M.</creatorcontrib><creatorcontrib>Palmer, Kyle</creatorcontrib><creatorcontrib>Bayne, Marvin</creatorcontrib><creatorcontrib>Monsma, Frederick J.</creatorcontrib><title>ADP Is the Cognate Ligand for the Orphan G Protein-coupled Receptor SP1999</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>P2Y receptors are a class of G protein-coupled receptors activated primarily by ATP, UTP, and UDP. Five mammalian P2Y receptors have been cloned so far including P2Y1, P2Y2, P2Y4, P2Y6, and P2Y11. P2Y1, P2Y2, and P2Y6 couple to the activation of phospholipase C, whereas P2Y4 and P2Y11 couple to the activation of both phospholipase C and the adenylyl cyclase pathways. Additional ADP receptors linked to Gαi have been described but have not yet been cloned. SP1999 is an orphan G protein-coupled receptor, which is highly expressed in brain, spinal cord, and blood platelets. In the present study, we demonstrate that SP1999 is a Gαi-coupled receptor that is potently activated by ADP. In an effort to identify ligands for SP1999, fractionated rat spinal cord extracts were assayed for Ca2+ mobilization activity against Chinese hamster ovary cells transiently transfected with SP1999 and chimeric Gα subunits (Gαq/i). A substance that selectively activated SP1999-transfected cells was identified and purified through a series of chromatographic steps. Mass spectral analysis of the purified material definitively identified it as ADP. ADP was subsequently shown to inhibit forskolin-stimulated adenylyl cyclase activity through selective activation of SP1999 with an EC50 of 60 nm. Other nucleotides were able to activate SP1999 with a rank order of potency 2-MeS-ATP = 2-MeS-ADP > ADP = adenosine 5′-O-2-(thio)diphosphate > 2-Cl-ATP > adenosine 5′-O-(thiotriphosphate). Thus, SP1999 is a novel, Gαi-linked receptor for ADP.AF321815</description><subject>3T3 Cells</subject><subject>Adenosine Diphosphate - metabolism</subject><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Base Sequence</subject><subject>CHO Cells</subject><subject>Cloning, Molecular</subject><subject>Cricetinae</subject><subject>DNA, Complementary - chemistry</subject><subject>Gene Expression Profiling</subject><subject>GTP-Binding Proteins - metabolism</subject><subject>Humans</subject><subject>Ligands</subject><subject>Mice</subject><subject>Molecular Sequence Data</subject><subject>Rats</subject><subject>Receptors, Purinergic P2 - metabolism</subject><subject>Receptors, Purinergic P2Y1</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kMFr2zAUh0VpabKs1x6LobCbU0mWLOlYsi3rSGnoWuhN2NJzrJBYruSs9L-vtgRy6rs8eHy_H48PoUuCpwQLdrOuzfQeYyWIpBifoDHBssgLTl5O0RhjSnJFuRyhLzGucRqmyDkaEUIwE4KN0e_b78vsLmZDC9nMr7pqgGzhVlVns8aH_-eH0LdVl82zZfADuC43ftdvwGaPYKAfEvVnSZRSX9FZU20iXBz2BD3__PE0-5UvHuZ3s9tFbphgQy5BUsMVWEsaxnhjy6KkJZe2sKriuKQUVCNxabmSjIiC1rZgoBjY2jLJWTFB3_a9ffCvO4iD3rpoYLOpOvC7qAWWAnPFEzjdgyb4GAM0ug9uW4V3TbD-Z08ne_poLwWuDs27egv2iB90JeB6D7Ru1b65ALp23rSw1VSUCdOyTPonSO4pSBb-Ogg6GgedAZsSZtDWu88--ABeTYYf</recordid><startdate>20010316</startdate><enddate>20010316</enddate><creator>Zhang, Fang L.</creator><creator>Luo, Lin</creator><creator>Gustafson, Eric</creator><creator>Lachowicz, Jean</creator><creator>Smith, Michelle</creator><creator>Qiao, Xudong</creator><creator>Liu, Yan-Hui</creator><creator>Chen, Guodong</creator><creator>Pramanik, Birendra</creator><creator>Laz, Thomas M.</creator><creator>Palmer, Kyle</creator><creator>Bayne, Marvin</creator><creator>Monsma, Frederick J.</creator><general>Elsevier Inc</general><general>American Society for Biochemistry and Molecular Biology</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20010316</creationdate><title>ADP Is the Cognate Ligand for the Orphan G Protein-coupled Receptor SP1999</title><author>Zhang, Fang L. ; Luo, Lin ; Gustafson, Eric ; Lachowicz, Jean ; Smith, Michelle ; Qiao, Xudong ; Liu, Yan-Hui ; Chen, Guodong ; Pramanik, Birendra ; Laz, Thomas M. ; Palmer, Kyle ; Bayne, Marvin ; Monsma, Frederick J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-8e82c59edd1f445fd6362658d3d9a50622e9f806d59841732bd34e94edbd48543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>3T3 Cells</topic><topic>Adenosine Diphosphate - metabolism</topic><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Base Sequence</topic><topic>CHO Cells</topic><topic>Cloning, Molecular</topic><topic>Cricetinae</topic><topic>DNA, Complementary - chemistry</topic><topic>Gene Expression Profiling</topic><topic>GTP-Binding Proteins - metabolism</topic><topic>Humans</topic><topic>Ligands</topic><topic>Mice</topic><topic>Molecular Sequence Data</topic><topic>Rats</topic><topic>Receptors, Purinergic P2 - metabolism</topic><topic>Receptors, Purinergic P2Y1</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Fang L.</creatorcontrib><creatorcontrib>Luo, Lin</creatorcontrib><creatorcontrib>Gustafson, Eric</creatorcontrib><creatorcontrib>Lachowicz, Jean</creatorcontrib><creatorcontrib>Smith, Michelle</creatorcontrib><creatorcontrib>Qiao, Xudong</creatorcontrib><creatorcontrib>Liu, Yan-Hui</creatorcontrib><creatorcontrib>Chen, Guodong</creatorcontrib><creatorcontrib>Pramanik, Birendra</creatorcontrib><creatorcontrib>Laz, Thomas M.</creatorcontrib><creatorcontrib>Palmer, Kyle</creatorcontrib><creatorcontrib>Bayne, Marvin</creatorcontrib><creatorcontrib>Monsma, Frederick J.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Fang L.</au><au>Luo, Lin</au><au>Gustafson, Eric</au><au>Lachowicz, Jean</au><au>Smith, Michelle</au><au>Qiao, Xudong</au><au>Liu, Yan-Hui</au><au>Chen, Guodong</au><au>Pramanik, Birendra</au><au>Laz, Thomas M.</au><au>Palmer, Kyle</au><au>Bayne, Marvin</au><au>Monsma, Frederick J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>ADP Is the Cognate Ligand for the Orphan G Protein-coupled Receptor SP1999</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>2001-03-16</date><risdate>2001</risdate><volume>276</volume><issue>11</issue><spage>8608</spage><epage>8615</epage><pages>8608-8615</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>P2Y receptors are a class of G protein-coupled receptors activated primarily by ATP, UTP, and UDP. Five mammalian P2Y receptors have been cloned so far including P2Y1, P2Y2, P2Y4, P2Y6, and P2Y11. P2Y1, P2Y2, and P2Y6 couple to the activation of phospholipase C, whereas P2Y4 and P2Y11 couple to the activation of both phospholipase C and the adenylyl cyclase pathways. Additional ADP receptors linked to Gαi have been described but have not yet been cloned. SP1999 is an orphan G protein-coupled receptor, which is highly expressed in brain, spinal cord, and blood platelets. In the present study, we demonstrate that SP1999 is a Gαi-coupled receptor that is potently activated by ADP. In an effort to identify ligands for SP1999, fractionated rat spinal cord extracts were assayed for Ca2+ mobilization activity against Chinese hamster ovary cells transiently transfected with SP1999 and chimeric Gα subunits (Gαq/i). A substance that selectively activated SP1999-transfected cells was identified and purified through a series of chromatographic steps. Mass spectral analysis of the purified material definitively identified it as ADP. ADP was subsequently shown to inhibit forskolin-stimulated adenylyl cyclase activity through selective activation of SP1999 with an EC50 of 60 nm. Other nucleotides were able to activate SP1999 with a rank order of potency 2-MeS-ATP = 2-MeS-ADP > ADP = adenosine 5′-O-2-(thio)diphosphate > 2-Cl-ATP > adenosine 5′-O-(thiotriphosphate). Thus, SP1999 is a novel, Gαi-linked receptor for ADP.AF321815</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>11104774</pmid><doi>10.1074/jbc.M009718200</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 3T3 Cells Adenosine Diphosphate - metabolism Amino Acid Sequence Animals Base Sequence CHO Cells Cloning, Molecular Cricetinae DNA, Complementary - chemistry Gene Expression Profiling GTP-Binding Proteins - metabolism Humans Ligands Mice Molecular Sequence Data Rats Receptors, Purinergic P2 - metabolism Receptors, Purinergic P2Y1 |
title | ADP Is the Cognate Ligand for the Orphan G Protein-coupled Receptor SP1999 |
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