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High-yield synthesis and purification of recombinant human GABA transaminase for high-throughput screening assays

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dc.contributor.authorMingu Gordon Park-
dc.contributor.authorAh-reum Han-
dc.contributor.authorSu Yeon Kim-
dc.contributor.authorTai Young Kim-
dc.contributor.authorHo Min Kim-
dc.contributor.authorC. Justin Lee-
dc.date.accessioned2021-09-28T04:30:15Z-
dc.date.accessioned2021-09-28T04:30:15Z-
dc.date.available2021-09-28T04:30:15Z-
dc.date.available2021-09-28T04:30:15Z-
dc.date.created2021-09-27-
dc.date.issued2021-01-01-
dc.identifier.issn1475-6366-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/10315-
dc.description.abstract© 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.Many studies have focussed on modulating the activity of γ-aminobutyric acid transaminase (GABA-T), a GABA-catabolizing enzyme, for treating neurological diseases, such as epilepsy and drug addiction. Nevertheless, human GABA-T synthesis and purification have not been established. Thus, biochemical and drug design studies on GABA-T have been performed by using porcine GABA-T mostly and even bacterial GABA-T. Here we report an optimised protocol for overexpression of 6xHis-tagged human GABA-T in human cells followed by a two-step protein purification. Then, we established an optimised human GABA-T (0.5 U/mg) activity assay. Finally, we compared the difference between human and bacterial GABA-T in sensitivity to two irreversible GABA-T inhibitors, gabaculine and vigabatrin. Human GABA-T in homodimeric form showed 70-fold higher sensitivity to vigabatrin than bacterial GABA-T in multimeric form, indicating the importance of using human GABA-T. In summary, our newly developed protocol can be an important first step in developing more effective human GABA-T modulators.-
dc.description.uri1-
dc.language영어-
dc.publisherTaylor and Francis Ltd.-
dc.titleHigh-yield synthesis and purification of recombinant human GABA transaminase for high-throughput screening assays-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000695129200001-
dc.identifier.scopusid2-s2.0-85114812910-
dc.identifier.rimsid76391-
dc.contributor.affiliatedAuthorMingu Gordon Park-
dc.contributor.affiliatedAuthorAh-reum Han-
dc.contributor.affiliatedAuthorSu Yeon Kim-
dc.contributor.affiliatedAuthorTai Young Kim-
dc.contributor.affiliatedAuthorHo Min Kim-
dc.contributor.affiliatedAuthorC. Justin Lee-
dc.identifier.doi10.1080/14756366.2021.1975697-
dc.identifier.bibliographicCitationJournal of Enzyme Inhibition and Medicinal Chemistry, v.36, no.1, pp.2016 - 2024-
dc.citation.titleJournal of Enzyme Inhibition and Medicinal Chemistry-
dc.citation.volume36-
dc.citation.number1-
dc.citation.startPage2016-
dc.citation.endPage2024-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Medicinal-
dc.subject.keywordPlusAMINOBUTYRIC-ACID AMINOTRANSFERASE-
dc.subject.keywordPlusGAMMA-VINYL GABA-
dc.subject.keywordPlusHUMAN-BRAIN-
dc.subject.keywordPlus4-AMINOBUTYRATE AMINOTRANSFERASE-
dc.subject.keywordPlusTISSUE DISTRIBUTION-
dc.subject.keywordPlusASTROCYTES-
dc.subject.keywordPlusINACTIVATION-
dc.subject.keywordPlusINHIBITION-
dc.subject.keywordPlusMECHANISM-
dc.subject.keywordPlusOVEREXPRESSION-
dc.subject.keywordAuthor4-Aminobutyrate transaminase-
dc.subject.keywordAuthorgabaculine-
dc.subject.keywordAuthorhigh-throughput screening assays-
dc.subject.keywordAuthorisolation and purification-
dc.subject.keywordAuthorvigabatrin-
Appears in Collections:
Center for Cognition and Sociality(인지 및 사회성 연구단) > 1. Journal Papers (저널논문)
Pioneer Research Center for Biomolecular and Cellular Structure(바이오분자 및 세포구조 연구단) > Protein Communication Group(단백질 커뮤니케이션 그룹) > 1. Journal Papers (저널논문)
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