Tissue-specific expression and gabapentin-binding properties of calcium channel alpha2delta subunit subtypes
We report here the tissue-specific expression and gabapentin-binding properties of calcium channel alpha2delta subunits. Northern blot analysis demonstrated that human alpha2delta-1, -2, and -3 mRNA all had high levels of expression in brain, heart and skeletal muscle. However, the highest expressio...
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Veröffentlicht in: | The Journal of membrane biology 2001-11, Vol.184 (1), p.35-43 |
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description | We report here the tissue-specific expression and gabapentin-binding properties of calcium channel alpha2delta subunits. Northern blot analysis demonstrated that human alpha2delta-1, -2, and -3 mRNA all had high levels of expression in brain, heart and skeletal muscle. However, the highest expression of human alpha2delta-2 mRNA was found in lung. Human alpha2delta-1, -2, and -3 mRNAs were detected in all portions of brain tested. Western blotting revealed that alpha2delta-2 protein was predominantly expressed in cerebellar cortex (brain) and undetectable in lung. The dissociation between mRNA and protein levels of human alpha2delta-2 in lung suggests possible post-transcriptional regulation. Although mouse alpha2delta-1 proteins exhibited a similar tissue distribution profile as that of human, tissue distribution of mouse alpha2delta-2 and -3 mRNA revealed a different profile. Mouse alpha2delta-3 mRNA was restricted to brain and mouse alpha2delta-2 mRNA was not detectable in lung. Gel electrophoresis under a reduced condition resulted in a mobility shift of both alpha2delta-1 and alpha2delta-2 proteins, suggesting that alpha2 and delta of alpha2delta-2 protein are linked by disulfide bond as are alpha2 and delta of alpha2delta-1. Scatchard plots revealed a single population of gabapentin binding sites for human alpha2delta-2 with the KD value twofold higher than that of porcine alpha2delta-1 (156 +/- 25 nm vs. 72 +/- 9 nm). Inhibition of gabapentin binding to alpha2delta-2 by selected amino acids and gabapentin analogs produced a binding profile similar, but not identical to that of alpha2delta-1. |
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Northern blot analysis demonstrated that human alpha2delta-1, -2, and -3 mRNA all had high levels of expression in brain, heart and skeletal muscle. However, the highest expression of human alpha2delta-2 mRNA was found in lung. Human alpha2delta-1, -2, and -3 mRNAs were detected in all portions of brain tested. Western blotting revealed that alpha2delta-2 protein was predominantly expressed in cerebellar cortex (brain) and undetectable in lung. The dissociation between mRNA and protein levels of human alpha2delta-2 in lung suggests possible post-transcriptional regulation. Although mouse alpha2delta-1 proteins exhibited a similar tissue distribution profile as that of human, tissue distribution of mouse alpha2delta-2 and -3 mRNA revealed a different profile. Mouse alpha2delta-3 mRNA was restricted to brain and mouse alpha2delta-2 mRNA was not detectable in lung. Gel electrophoresis under a reduced condition resulted in a mobility shift of both alpha2delta-1 and alpha2delta-2 proteins, suggesting that alpha2 and delta of alpha2delta-2 protein are linked by disulfide bond as are alpha2 and delta of alpha2delta-1. Scatchard plots revealed a single population of gabapentin binding sites for human alpha2delta-2 with the KD value twofold higher than that of porcine alpha2delta-1 (156 +/- 25 nm vs. 72 +/- 9 nm). Inhibition of gabapentin binding to alpha2delta-2 by selected amino acids and gabapentin analogs produced a binding profile similar, but not identical to that of alpha2delta-1.</description><identifier>ISSN: 0022-2631</identifier><identifier>PMID: 11687876</identifier><language>eng</language><publisher>United States</publisher><subject>Acetates - metabolism ; Amines ; Amino Acids - metabolism ; Animals ; Anticonvulsants - metabolism ; Binding Sites ; Calcium Channels - chemistry ; Calcium Channels - genetics ; Calcium Channels - metabolism ; Cell Line ; Cyclohexanecarboxylic Acids ; Gabapentin ; gamma-Aminobutyric Acid ; Humans ; Mice ; Protein Binding ; Protein Isoforms ; Protein Structure, Secondary ; Protein Subunits ; Radioligand Assay ; Tissue Distribution</subject><ispartof>The Journal of membrane biology, 2001-11, Vol.184 (1), p.35-43</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11687876$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gong, H C</creatorcontrib><creatorcontrib>Hang, J</creatorcontrib><creatorcontrib>Kohler, W</creatorcontrib><creatorcontrib>Li, L</creatorcontrib><creatorcontrib>Su, T Z</creatorcontrib><title>Tissue-specific expression and gabapentin-binding properties of calcium channel alpha2delta subunit subtypes</title><title>The Journal of membrane biology</title><addtitle>J Membr Biol</addtitle><description>We report here the tissue-specific expression and gabapentin-binding properties of calcium channel alpha2delta subunits. Northern blot analysis demonstrated that human alpha2delta-1, -2, and -3 mRNA all had high levels of expression in brain, heart and skeletal muscle. However, the highest expression of human alpha2delta-2 mRNA was found in lung. Human alpha2delta-1, -2, and -3 mRNAs were detected in all portions of brain tested. Western blotting revealed that alpha2delta-2 protein was predominantly expressed in cerebellar cortex (brain) and undetectable in lung. The dissociation between mRNA and protein levels of human alpha2delta-2 in lung suggests possible post-transcriptional regulation. Although mouse alpha2delta-1 proteins exhibited a similar tissue distribution profile as that of human, tissue distribution of mouse alpha2delta-2 and -3 mRNA revealed a different profile. Mouse alpha2delta-3 mRNA was restricted to brain and mouse alpha2delta-2 mRNA was not detectable in lung. Gel electrophoresis under a reduced condition resulted in a mobility shift of both alpha2delta-1 and alpha2delta-2 proteins, suggesting that alpha2 and delta of alpha2delta-2 protein are linked by disulfide bond as are alpha2 and delta of alpha2delta-1. Scatchard plots revealed a single population of gabapentin binding sites for human alpha2delta-2 with the KD value twofold higher than that of porcine alpha2delta-1 (156 +/- 25 nm vs. 72 +/- 9 nm). Inhibition of gabapentin binding to alpha2delta-2 by selected amino acids and gabapentin analogs produced a binding profile similar, but not identical to that of alpha2delta-1.</description><subject>Acetates - metabolism</subject><subject>Amines</subject><subject>Amino Acids - metabolism</subject><subject>Animals</subject><subject>Anticonvulsants - metabolism</subject><subject>Binding Sites</subject><subject>Calcium Channels - chemistry</subject><subject>Calcium Channels - genetics</subject><subject>Calcium Channels - metabolism</subject><subject>Cell Line</subject><subject>Cyclohexanecarboxylic Acids</subject><subject>Gabapentin</subject><subject>gamma-Aminobutyric Acid</subject><subject>Humans</subject><subject>Mice</subject><subject>Protein Binding</subject><subject>Protein Isoforms</subject><subject>Protein Structure, Secondary</subject><subject>Protein Subunits</subject><subject>Radioligand Assay</subject><subject>Tissue Distribution</subject><issn>0022-2631</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1kE1LxDAURbNQnHH0L0hW7gpJmjbtUga_YMCFsy8vzetMJE1jXwPOv3dE5S7O5nC53Au2FkKpQtWlXLFrog8hpDG1vmIrKevGNKZes7D3RBkLStj7wfccv9KMRH6KHKLjB7CQMC4-FtZH5-OBp3lKOC8eiU8D7yH0Po-8P0KMGDiEdATlMCzAKdsc_fLD5ZSQbtjlAIHw9o8b9v70uN--FLu359ftw644mLYuqsoo7YzTOOiqbVE4K4wQFi1qbIUVdYVgSrRSt1paLRotpVatFEMDbig37P639Tz0MyMt3eipxxAg4pSpM0pV55Rn8e5PzHZE16XZjzCfuv93ym_MBWIR</recordid><startdate>20011101</startdate><enddate>20011101</enddate><creator>Gong, H C</creator><creator>Hang, J</creator><creator>Kohler, W</creator><creator>Li, L</creator><creator>Su, T Z</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>20011101</creationdate><title>Tissue-specific expression and gabapentin-binding properties of calcium channel alpha2delta subunit subtypes</title><author>Gong, H C ; Hang, J ; Kohler, W ; Li, L ; Su, T Z</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-g796-55724d7d4ef4599e0db0700bebe4e90b065ea73eb14941b40841142910f8adf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Acetates - metabolism</topic><topic>Amines</topic><topic>Amino Acids - metabolism</topic><topic>Animals</topic><topic>Anticonvulsants - metabolism</topic><topic>Binding Sites</topic><topic>Calcium Channels - chemistry</topic><topic>Calcium Channels - genetics</topic><topic>Calcium Channels - metabolism</topic><topic>Cell Line</topic><topic>Cyclohexanecarboxylic Acids</topic><topic>Gabapentin</topic><topic>gamma-Aminobutyric Acid</topic><topic>Humans</topic><topic>Mice</topic><topic>Protein Binding</topic><topic>Protein Isoforms</topic><topic>Protein Structure, Secondary</topic><topic>Protein Subunits</topic><topic>Radioligand Assay</topic><topic>Tissue Distribution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gong, H C</creatorcontrib><creatorcontrib>Hang, J</creatorcontrib><creatorcontrib>Kohler, W</creatorcontrib><creatorcontrib>Li, L</creatorcontrib><creatorcontrib>Su, T Z</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>The Journal of membrane biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gong, H C</au><au>Hang, J</au><au>Kohler, W</au><au>Li, L</au><au>Su, T Z</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tissue-specific expression and gabapentin-binding properties of calcium channel alpha2delta subunit subtypes</atitle><jtitle>The Journal of membrane biology</jtitle><addtitle>J Membr Biol</addtitle><date>2001-11-01</date><risdate>2001</risdate><volume>184</volume><issue>1</issue><spage>35</spage><epage>43</epage><pages>35-43</pages><issn>0022-2631</issn><abstract>We report here the tissue-specific expression and gabapentin-binding properties of calcium channel alpha2delta subunits. Northern blot analysis demonstrated that human alpha2delta-1, -2, and -3 mRNA all had high levels of expression in brain, heart and skeletal muscle. However, the highest expression of human alpha2delta-2 mRNA was found in lung. Human alpha2delta-1, -2, and -3 mRNAs were detected in all portions of brain tested. Western blotting revealed that alpha2delta-2 protein was predominantly expressed in cerebellar cortex (brain) and undetectable in lung. The dissociation between mRNA and protein levels of human alpha2delta-2 in lung suggests possible post-transcriptional regulation. Although mouse alpha2delta-1 proteins exhibited a similar tissue distribution profile as that of human, tissue distribution of mouse alpha2delta-2 and -3 mRNA revealed a different profile. Mouse alpha2delta-3 mRNA was restricted to brain and mouse alpha2delta-2 mRNA was not detectable in lung. Gel electrophoresis under a reduced condition resulted in a mobility shift of both alpha2delta-1 and alpha2delta-2 proteins, suggesting that alpha2 and delta of alpha2delta-2 protein are linked by disulfide bond as are alpha2 and delta of alpha2delta-1. Scatchard plots revealed a single population of gabapentin binding sites for human alpha2delta-2 with the KD value twofold higher than that of porcine alpha2delta-1 (156 +/- 25 nm vs. 72 +/- 9 nm). Inhibition of gabapentin binding to alpha2delta-2 by selected amino acids and gabapentin analogs produced a binding profile similar, but not identical to that of alpha2delta-1.</abstract><cop>United States</cop><pmid>11687876</pmid><tpages>9</tpages></addata></record> |
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subjects | Acetates - metabolism Amines Amino Acids - metabolism Animals Anticonvulsants - metabolism Binding Sites Calcium Channels - chemistry Calcium Channels - genetics Calcium Channels - metabolism Cell Line Cyclohexanecarboxylic Acids Gabapentin gamma-Aminobutyric Acid Humans Mice Protein Binding Protein Isoforms Protein Structure, Secondary Protein Subunits Radioligand Assay Tissue Distribution |
title | Tissue-specific expression and gabapentin-binding properties of calcium channel alpha2delta subunit subtypes |
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