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dc.contributor.authorChoi, Yun Hee-
dc.contributor.authorKang, Hatan-
dc.contributor.authorLee, Won Kyu-
dc.contributor.authorKim, Taehyun-
dc.contributor.authorRhim, Hyewhon-
dc.contributor.authorYu, Yeon Gyu-
dc.date.accessioned2024-01-21T01:00:43Z-
dc.date.available2024-01-21T01:00:43Z-
dc.date.created2022-01-10-
dc.date.issued2007-06-30-
dc.identifier.issn1226-3613-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/134308-
dc.description.abstractSerotonin receptor subtype 6 (5-HT6) is a neurotransmitter receptor, which is involved in various brain functions such as memory and mood. It mediates signaling via the interaction with a stimulatory G-protein. Especially, the third intracellular loop (iL3) of 5-HT6 and the alpha subunit of stimulatory G protein (G alpha(s)) are responsible for the signaling process of 5-HT6. Chemical compounds that could inhibit the interaction between the iL3 region of 5-HT6 and Get, were screened from a chemical library consisted of 5,600 synthetic compounds. One of the identified compounds bound to G alpha(s) and effectively blocked the interaction between G alpha(s) and the iL3 region of 5-HT6. The identified compound was further shown to reduce the serotonin-induced accumulation of cAMP in 293T cells transformed with 5-HT6 cDNA. It also lowered the Ca2+ efflux induced by serotonin in cells expressing 5-HT6 and chimeric G alpha(s5/q). These results indicate that the interaction between the iL3 of 5-HT6 and G alpha(s) can be exploited for screening of regulatory compounds against the signaling pathway of 5-HT6.-
dc.languageEnglish-
dc.publisherNATURE PUBLISHING GROUP-
dc.subjectPHARMACOLOGICAL CHARACTERIZATION-
dc.subject5-HYDROXYTRYPTAMINE RECEPTOR-
dc.subjectADENYLATE-CYCLASE-
dc.subjectBINDING SITES-
dc.subjectRAT-
dc.subjectEXPRESSION-
dc.subjectCLONING-
dc.subjectCLASSIFICATION-
dc.subjectNOMENCLATURE-
dc.subjectRADIOLIGAND-
dc.titleAn inhibitory compound against the interaction between Gas and the third intracellular loop region of serotonin receptor subtype 6 (5-HT6) disrupts the signaling pathway of 5-HT6-
dc.typeArticle-
dc.identifier.doi10.1038/emm.2007.37-
dc.description.journalClass1-
dc.identifier.bibliographicCitationEXPERIMENTAL AND MOLECULAR MEDICINE, v.39, no.3, pp.335 - 342-
dc.citation.titleEXPERIMENTAL AND MOLECULAR MEDICINE-
dc.citation.volume39-
dc.citation.number3-
dc.citation.startPage335-
dc.citation.endPage342-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.identifier.kciidART001059165-
dc.identifier.wosid000247798800010-
dc.identifier.scopusid2-s2.0-34447130218-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryMedicine, Research & Experimental-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaResearch & Experimental Medicine-
dc.type.docTypeArticle-
dc.subject.keywordPlusPHARMACOLOGICAL CHARACTERIZATION-
dc.subject.keywordPlus5-HYDROXYTRYPTAMINE RECEPTOR-
dc.subject.keywordPlusADENYLATE-CYCLASE-
dc.subject.keywordPlusBINDING SITES-
dc.subject.keywordPlusRAT-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusCLONING-
dc.subject.keywordPlusCLASSIFICATION-
dc.subject.keywordPlusNOMENCLATURE-
dc.subject.keywordPlusRADIOLIGAND-
dc.subject.keywordAuthorgTP-binding protein asubunits-
dc.subject.keywordAuthorGs-
dc.subject.keywordAuthorserotonin-
dc.subject.keywordAuthorserotonin 6 receptor-
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