Applications of yeast-based signaling sensor for characterization of antagonist and analysis of site-directed mutants of the human serotonin 1A receptor
ABSTRACT The monoamine neurotransmitter serotonin (5‐HT) regulates a wide spectrum of human physiology through the 5‐HT receptor family. One such receptor, the 5‐HT1A receptor (HTR1A), is the most widely studied subtype and represents a significant molecular target in medicinal and therapeutic field...
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creator | Nakamura, Yasuyuki Ishii, Jun Kondo, Akihiko |
description | ABSTRACT
The monoamine neurotransmitter serotonin (5‐HT) regulates a wide spectrum of human physiology through the 5‐HT receptor family. One such receptor, the 5‐HT1A receptor (HTR1A), is the most widely studied subtype and represents a significant molecular target in medicinal and therapeutic fields. Yeast‐based fluorescent reporter systems have proven to be especially useful for GPCR assays, since detection using a fluorescent reporter considerably simplifies measurement procedures. However, previously reported systems using enhanced green fluorescent protein (EGFP) as the reporter in yeast still showed low signal‐to‐noise (S/N) ratios, making EGFP difficult to apply as an easily accessible tool. Therefore, we constructed a refined yeast‐based GPCR biosensor employing a high‐sensitivity strain that incorporated both a Gα‐engineered receptor and a fluorescent reporter (ZsGreen). As we report here, the refined yeast‐based fluorescent biosensor was applied successfully to antagonist characterization and analysis of site‐directed mutants of the HTR1A receptor. Pindolol, a known antagonist of HTR1A, specifically inhibited agonist‐induced signaling, demonstrating the ease of evaluating inhibition effects using our reporter strain. Characterization of site‐specific receptor mutants confirmed the role of specific targeted residues, including the highly conserved DRY motif, in the activation of HTR1A. Thus, our refined yeast biosensor strain, which incorporates a ZsGreen reporter and an engineered Gα receptor, is expected to serve as a simple and practical sensing tool for evaluating the ligand candidates and defining residues important to the function of human GPCRs. Biotechnol. Bioeng. 2015;112: 1906–1915. © 2015 Wiley Periodicals, Inc.
In this work, a yeast‐based signaling biosensor for human serotonin 1A receptor (HTR1A) was generated. In this biosensor, a ZsGreen fluorescence reporter gene‐based assay allowed the simple detection of agonist‐promoted signaling. Furthermore, the authors successfully applied the yeast biosensor strain for the characterization of antagonist and the analysis of site‐directed mutants of the human HTR1A receptor. |
doi_str_mv | 10.1002/bit.25597 |
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The monoamine neurotransmitter serotonin (5‐HT) regulates a wide spectrum of human physiology through the 5‐HT receptor family. One such receptor, the 5‐HT1A receptor (HTR1A), is the most widely studied subtype and represents a significant molecular target in medicinal and therapeutic fields. Yeast‐based fluorescent reporter systems have proven to be especially useful for GPCR assays, since detection using a fluorescent reporter considerably simplifies measurement procedures. However, previously reported systems using enhanced green fluorescent protein (EGFP) as the reporter in yeast still showed low signal‐to‐noise (S/N) ratios, making EGFP difficult to apply as an easily accessible tool. Therefore, we constructed a refined yeast‐based GPCR biosensor employing a high‐sensitivity strain that incorporated both a Gα‐engineered receptor and a fluorescent reporter (ZsGreen). As we report here, the refined yeast‐based fluorescent biosensor was applied successfully to antagonist characterization and analysis of site‐directed mutants of the HTR1A receptor. Pindolol, a known antagonist of HTR1A, specifically inhibited agonist‐induced signaling, demonstrating the ease of evaluating inhibition effects using our reporter strain. Characterization of site‐specific receptor mutants confirmed the role of specific targeted residues, including the highly conserved DRY motif, in the activation of HTR1A. Thus, our refined yeast biosensor strain, which incorporates a ZsGreen reporter and an engineered Gα receptor, is expected to serve as a simple and practical sensing tool for evaluating the ligand candidates and defining residues important to the function of human GPCRs. Biotechnol. Bioeng. 2015;112: 1906–1915. © 2015 Wiley Periodicals, Inc.
In this work, a yeast‐based signaling biosensor for human serotonin 1A receptor (HTR1A) was generated. In this biosensor, a ZsGreen fluorescence reporter gene‐based assay allowed the simple detection of agonist‐promoted signaling. Furthermore, the authors successfully applied the yeast biosensor strain for the characterization of antagonist and the analysis of site‐directed mutants of the human HTR1A receptor.</description><identifier>ISSN: 0006-3592</identifier><identifier>EISSN: 1097-0290</identifier><identifier>DOI: 10.1002/bit.25597</identifier><identifier>PMID: 25850571</identifier><identifier>CODEN: BIBIAU</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>Assaying ; Bioengineering ; Biosensors ; G-protein signaling ; G-protein-coupled receptor ; green fluorescent protein ; Green Fluorescent Proteins - chemistry ; Green Fluorescent Proteins - genetics ; Green Fluorescent Proteins - metabolism ; Human ; Humans ; mutagenesis ; Mutagenesis, Site-Directed - methods ; Mutation ; Neurotransmitters ; Plasmids ; Proteins ; Receptor, Serotonin, 5-HT1A - chemistry ; Receptor, Serotonin, 5-HT1A - genetics ; Receptor, Serotonin, 5-HT1A - metabolism ; Receptors ; Saccharomyces cerevisiae ; Saccharomyces cerevisiae - chemistry ; Saccharomyces cerevisiae - genetics ; Saccharomyces cerevisiae - metabolism ; Serotonin ; serotonin 1A receptor ; Serotonin 5-HT1 Receptor Antagonists - metabolism ; Signal Transduction ; Strain ; Yeast ; Yeasts</subject><ispartof>Biotechnology and bioengineering, 2015-09, Vol.112 (9), p.1906-1915</ispartof><rights>2015 Wiley Periodicals, Inc.</rights><rights>Copyright Wiley Subscription Services, Inc. Sep 2015</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c6307-e472b6e890a1cd6d7b26537a53549b9fd6bf83d486eaef34d2b850df00c00b023</citedby><cites>FETCH-LOGICAL-c6307-e472b6e890a1cd6d7b26537a53549b9fd6bf83d486eaef34d2b850df00c00b023</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fbit.25597$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fbit.25597$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25850571$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nakamura, Yasuyuki</creatorcontrib><creatorcontrib>Ishii, Jun</creatorcontrib><creatorcontrib>Kondo, Akihiko</creatorcontrib><title>Applications of yeast-based signaling sensor for characterization of antagonist and analysis of site-directed mutants of the human serotonin 1A receptor</title><title>Biotechnology and bioengineering</title><addtitle>Biotechnol. Bioeng</addtitle><description>ABSTRACT
The monoamine neurotransmitter serotonin (5‐HT) regulates a wide spectrum of human physiology through the 5‐HT receptor family. One such receptor, the 5‐HT1A receptor (HTR1A), is the most widely studied subtype and represents a significant molecular target in medicinal and therapeutic fields. Yeast‐based fluorescent reporter systems have proven to be especially useful for GPCR assays, since detection using a fluorescent reporter considerably simplifies measurement procedures. However, previously reported systems using enhanced green fluorescent protein (EGFP) as the reporter in yeast still showed low signal‐to‐noise (S/N) ratios, making EGFP difficult to apply as an easily accessible tool. Therefore, we constructed a refined yeast‐based GPCR biosensor employing a high‐sensitivity strain that incorporated both a Gα‐engineered receptor and a fluorescent reporter (ZsGreen). As we report here, the refined yeast‐based fluorescent biosensor was applied successfully to antagonist characterization and analysis of site‐directed mutants of the HTR1A receptor. Pindolol, a known antagonist of HTR1A, specifically inhibited agonist‐induced signaling, demonstrating the ease of evaluating inhibition effects using our reporter strain. Characterization of site‐specific receptor mutants confirmed the role of specific targeted residues, including the highly conserved DRY motif, in the activation of HTR1A. Thus, our refined yeast biosensor strain, which incorporates a ZsGreen reporter and an engineered Gα receptor, is expected to serve as a simple and practical sensing tool for evaluating the ligand candidates and defining residues important to the function of human GPCRs. Biotechnol. Bioeng. 2015;112: 1906–1915. © 2015 Wiley Periodicals, Inc.
In this work, a yeast‐based signaling biosensor for human serotonin 1A receptor (HTR1A) was generated. In this biosensor, a ZsGreen fluorescence reporter gene‐based assay allowed the simple detection of agonist‐promoted signaling. Furthermore, the authors successfully applied the yeast biosensor strain for the characterization of antagonist and the analysis of site‐directed mutants of the human HTR1A receptor.</description><subject>Assaying</subject><subject>Bioengineering</subject><subject>Biosensors</subject><subject>G-protein signaling</subject><subject>G-protein-coupled receptor</subject><subject>green fluorescent protein</subject><subject>Green Fluorescent Proteins - chemistry</subject><subject>Green Fluorescent Proteins - genetics</subject><subject>Green Fluorescent Proteins - metabolism</subject><subject>Human</subject><subject>Humans</subject><subject>mutagenesis</subject><subject>Mutagenesis, Site-Directed - methods</subject><subject>Mutation</subject><subject>Neurotransmitters</subject><subject>Plasmids</subject><subject>Proteins</subject><subject>Receptor, Serotonin, 5-HT1A - chemistry</subject><subject>Receptor, Serotonin, 5-HT1A - genetics</subject><subject>Receptor, Serotonin, 5-HT1A - metabolism</subject><subject>Receptors</subject><subject>Saccharomyces cerevisiae</subject><subject>Saccharomyces cerevisiae - chemistry</subject><subject>Saccharomyces cerevisiae - genetics</subject><subject>Saccharomyces cerevisiae - metabolism</subject><subject>Serotonin</subject><subject>serotonin 1A receptor</subject><subject>Serotonin 5-HT1 Receptor Antagonists - metabolism</subject><subject>Signal Transduction</subject><subject>Strain</subject><subject>Yeast</subject><subject>Yeasts</subject><issn>0006-3592</issn><issn>1097-0290</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc1u1DAURi0EokNhwQugSGxgkfY6iX-yHEYwFBVYMKhLy4lvZlwycbAdwfAkPC5upu0CCYnFlW35nE-yP0KeUzijAMV5Y-NZwVgtHpAFhVrkUNTwkCwAgOclq4sT8iSE63QUkvPH5KRgkgETdEF-L8ext62O1g0hc112QB1i3uiAJgt2O-jeDtss4BCcz7o07U573Ub09tds3Uh6iHrrBhti2po0uj8EO-cFGzE31mNSTLafYmLni7jDbDft9ZDCvYvJHjK6zBKIY3T-KXnU6T7gs9v1lHx993azep9ffl5frJaXectLEDlWomg4yho0bQ03oik4K4VmJavqpu4MbzpZmkpy1NiVlSma9HTTAbQADRTlKXl1zB29-z5hiGpvQ4t9rwd0U1BUUFkLJv8LBQaSV1Qm9OVf6LWbfPqWmaKcUgY8Ua-PVOtdCB47NXq71_6gKKibZlVqVs3NJvbFbeLU7NHck3dVJuD8CPywPR7-naTeXGzuIvOjkXrDn_eG9t8UF6Vg6urTWn1Yf_wirzYrBeUfjPq-SA</recordid><startdate>201509</startdate><enddate>201509</enddate><creator>Nakamura, Yasuyuki</creator><creator>Ishii, Jun</creator><creator>Kondo, Akihiko</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</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>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7T7</scope><scope>7TA</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><scope>M7N</scope></search><sort><creationdate>201509</creationdate><title>Applications of yeast-based signaling sensor for characterization of antagonist and analysis of site-directed mutants of the human serotonin 1A receptor</title><author>Nakamura, Yasuyuki ; Ishii, Jun ; Kondo, Akihiko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6307-e472b6e890a1cd6d7b26537a53549b9fd6bf83d486eaef34d2b850df00c00b023</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Assaying</topic><topic>Bioengineering</topic><topic>Biosensors</topic><topic>G-protein signaling</topic><topic>G-protein-coupled receptor</topic><topic>green fluorescent protein</topic><topic>Green Fluorescent Proteins - chemistry</topic><topic>Green Fluorescent Proteins - genetics</topic><topic>Green Fluorescent Proteins - metabolism</topic><topic>Human</topic><topic>Humans</topic><topic>mutagenesis</topic><topic>Mutagenesis, Site-Directed - methods</topic><topic>Mutation</topic><topic>Neurotransmitters</topic><topic>Plasmids</topic><topic>Proteins</topic><topic>Receptor, Serotonin, 5-HT1A - chemistry</topic><topic>Receptor, Serotonin, 5-HT1A - genetics</topic><topic>Receptor, Serotonin, 5-HT1A - metabolism</topic><topic>Receptors</topic><topic>Saccharomyces cerevisiae</topic><topic>Saccharomyces cerevisiae - chemistry</topic><topic>Saccharomyces cerevisiae - genetics</topic><topic>Saccharomyces cerevisiae - metabolism</topic><topic>Serotonin</topic><topic>serotonin 1A receptor</topic><topic>Serotonin 5-HT1 Receptor Antagonists - metabolism</topic><topic>Signal Transduction</topic><topic>Strain</topic><topic>Yeast</topic><topic>Yeasts</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nakamura, Yasuyuki</creatorcontrib><creatorcontrib>Ishii, Jun</creatorcontrib><creatorcontrib>Kondo, Akihiko</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Materials Business File</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><jtitle>Biotechnology and bioengineering</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nakamura, Yasuyuki</au><au>Ishii, Jun</au><au>Kondo, Akihiko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Applications of yeast-based signaling sensor for characterization of antagonist and analysis of site-directed mutants of the human serotonin 1A receptor</atitle><jtitle>Biotechnology and bioengineering</jtitle><addtitle>Biotechnol. Bioeng</addtitle><date>2015-09</date><risdate>2015</risdate><volume>112</volume><issue>9</issue><spage>1906</spage><epage>1915</epage><pages>1906-1915</pages><issn>0006-3592</issn><eissn>1097-0290</eissn><coden>BIBIAU</coden><abstract>ABSTRACT
The monoamine neurotransmitter serotonin (5‐HT) regulates a wide spectrum of human physiology through the 5‐HT receptor family. One such receptor, the 5‐HT1A receptor (HTR1A), is the most widely studied subtype and represents a significant molecular target in medicinal and therapeutic fields. Yeast‐based fluorescent reporter systems have proven to be especially useful for GPCR assays, since detection using a fluorescent reporter considerably simplifies measurement procedures. However, previously reported systems using enhanced green fluorescent protein (EGFP) as the reporter in yeast still showed low signal‐to‐noise (S/N) ratios, making EGFP difficult to apply as an easily accessible tool. Therefore, we constructed a refined yeast‐based GPCR biosensor employing a high‐sensitivity strain that incorporated both a Gα‐engineered receptor and a fluorescent reporter (ZsGreen). As we report here, the refined yeast‐based fluorescent biosensor was applied successfully to antagonist characterization and analysis of site‐directed mutants of the HTR1A receptor. Pindolol, a known antagonist of HTR1A, specifically inhibited agonist‐induced signaling, demonstrating the ease of evaluating inhibition effects using our reporter strain. Characterization of site‐specific receptor mutants confirmed the role of specific targeted residues, including the highly conserved DRY motif, in the activation of HTR1A. Thus, our refined yeast biosensor strain, which incorporates a ZsGreen reporter and an engineered Gα receptor, is expected to serve as a simple and practical sensing tool for evaluating the ligand candidates and defining residues important to the function of human GPCRs. Biotechnol. Bioeng. 2015;112: 1906–1915. © 2015 Wiley Periodicals, Inc.
In this work, a yeast‐based signaling biosensor for human serotonin 1A receptor (HTR1A) was generated. In this biosensor, a ZsGreen fluorescence reporter gene‐based assay allowed the simple detection of agonist‐promoted signaling. Furthermore, the authors successfully applied the yeast biosensor strain for the characterization of antagonist and the analysis of site‐directed mutants of the human HTR1A receptor.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>25850571</pmid><doi>10.1002/bit.25597</doi><tpages>10</tpages></addata></record> |
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subjects | Assaying Bioengineering Biosensors G-protein signaling G-protein-coupled receptor green fluorescent protein Green Fluorescent Proteins - chemistry Green Fluorescent Proteins - genetics Green Fluorescent Proteins - metabolism Human Humans mutagenesis Mutagenesis, Site-Directed - methods Mutation Neurotransmitters Plasmids Proteins Receptor, Serotonin, 5-HT1A - chemistry Receptor, Serotonin, 5-HT1A - genetics Receptor, Serotonin, 5-HT1A - metabolism Receptors Saccharomyces cerevisiae Saccharomyces cerevisiae - chemistry Saccharomyces cerevisiae - genetics Saccharomyces cerevisiae - metabolism Serotonin serotonin 1A receptor Serotonin 5-HT1 Receptor Antagonists - metabolism Signal Transduction Strain Yeast Yeasts |
title | Applications of yeast-based signaling sensor for characterization of antagonist and analysis of site-directed mutants of the human serotonin 1A receptor |
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