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dc.contributor.authorWubshet, Sileshi Gizachhew
dc.contributor.authorLiu, Bingrui
dc.contributor.authorKongstad, Kenneth T.
dc.contributor.authorBöcker, Ulrike
dc.contributor.authorPetersen, Malene J.
dc.contributor.authorLi, Tuo
dc.contributor.authorWang, Junru
dc.contributor.authorStaerk, Dan
dc.date.accessioned2019-04-03T08:48:15Z
dc.date.available2019-04-03T08:48:15Z
dc.date.created2019-03-28T13:26:10Z
dc.date.issued2019
dc.identifier.citationTalanta: The International Journal of Pure and Applied Analytical Chemistry. 2019, 200 279-287.nb_NO
dc.identifier.issn0039-9140
dc.identifier.urihttp://hdl.handle.net/11250/2593069
dc.description.abstractPlants are well-recognized sources of inhibitors for -glucosidase - a key target enzyme for management of type 2 diabetes. Recently, two advanced bioactivity-profiling techniques, i.e., ligand fishing and high-resolution inhibition profiling, have shown great promises for accelerating identification of -glucosidase inhibitors from complex plant extracts. Non-specific affinities and non-specific inhibitions are major sources of false positive hits from ligand fishing and highresolution inhibition profiling, respectively. In an attempt to minimize such false positive hits, we describe a new screening approach based on ligand fishing and high-resolution inhibition profiling for detection of high-affinity ligands and assessment of inhibitory activity, respectively. The complementary nature of ligand fishing and high-resolution inhibition profiling was explored to Manuscript for Talanta 3 identify-glucosidase inhibitory ligands from a complex mixture, and proof-of-concept was demonstrated with crude ethyl acetate extract of Ginkgo biloba. In addition to magnetic beads with a 3-carbon aliphatic linker, -glucosidase was immobilized on magnetic beads with a 21-carbon aliphatic linker; and the two different types of magnetic beads were compared for their hydrolytic activity and fishing efficiency.
dc.language.isoengnb_NO
dc.titleCombined magnetic ligand fishing and high-resolution inhibition profiling for identification of α-glucosidase inhibitory ligands: A new screening approach based on complimentary inhibition and affinity profilesnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionacceptedVersion
dc.description.versionpublishedVersion
dc.source.pagenumber279-287nb_NO
dc.source.volume200nb_NO
dc.source.journalTalanta: The International Journal of Pure and Applied Analytical Chemistrynb_NO
dc.identifier.doi10.1016/j.talanta.2019.03.047
dc.identifier.cristin1688554
dc.relation.projectNorges forskningsråd: 262308nb_NO
dc.relation.projectNorges forskningsråd: 261849nb_NO
cristin.unitcode7543,3,2,0
cristin.unitnameRåvare og prosess
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.fulltextoriginal
cristin.qualitycode1


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