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
Hauptverfasser: 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.
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container_end_page 8615
container_issue 11
container_start_page 8608
container_title The Journal of biological chemistry
container_volume 276
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 &gt; ADP = adenosine 5′-O-2-(thio)diphosphate &gt; 2-Cl-ATP &gt; adenosine 5′-O-(thiotriphosphate). 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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. 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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 &gt; ADP = adenosine 5′-O-2-(thio)diphosphate &gt; 2-Cl-ATP &gt; adenosine 5′-O-(thiotriphosphate). 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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 &gt; ADP = adenosine 5′-O-2-(thio)diphosphate &gt; 2-Cl-ATP &gt; 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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