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dc.contributor.authorSumalee Kamchonwongpaisanen_US
dc.contributor.authorJarunee Vanichtanankulen_US
dc.contributor.authorBongkoch Tarnchompooen_US
dc.contributor.authorJirundon Yuvaniyamaen_US
dc.contributor.authorSupannee Taweechaien_US
dc.contributor.authorYongyuth Yuthavongen_US
dc.contributor.otherThailand National Center for Genetic Engineering and Biotechnologyen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-06-21T08:12:25Z-
dc.date.available2018-06-21T08:12:25Z-
dc.date.issued2005-03-01en_US
dc.identifier.citationAnalytical Chemistry. Vol.77, No.5 (2005), 1222-1227en_US
dc.identifier.issn00032700en_US
dc.identifier.other2-s2.0-14744274646en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=14744274646&origin=inwarden_US
dc.identifier.urihttp://repository.li.mahidol.ac.th/dspace/handle/123456789/16449-
dc.description.abstractA simple method for screening combinatorial and other libraries of inhibitors of malarial (Plasmodium falciparum) dihydrofolate reductase (PfDHFR) has been developed, based on the affinities of the inhibitors with the enzyme. In the presence of limiting amounts of the enzyme, a number of inhibitors in the library were bound to extents reflecting the relative binding affinities. Following ultrafiltration and guanidine hydrochloride treatment to release bound inhibitors, the amounts of free and bound inhibitors could be determined by high-performance liquid chromatography and liquid chromatography-mass spectrometry. The differences in the patterns reflected the binding of high-affinity components compared with the other members in the library. A good correlation was found between the inhibition constants (Ki values) and the extent of binding of inhibitors to wild-type, double (C59R+S108N) and quadruple mutant (N51I+ C59R+S108N+I164L) of PfDHFR, as well as human DHFR. In addition to identifying lead components of the libraries with high affinities (low Ki values) and stabilities (low koff rates), this simple method also provides an alternative way for quickly and accurately calculating enzyme binding affinities of inhibitors in combinatorial chemical libraries. © 2005 American Chemical Society.en_US
dc.rightsMahidol Universityen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=14744274646&origin=inwarden_US
dc.subjectChemistryen_US
dc.titleStoichiometric selection of tight-binding inhibitors by wild-type mutant forms of malarial (Plasmodium falciparum) dihydrofolate reductaseen_US
dc.typeArticleen_US
dc.rights.holderSCOPUSen_US
dc.identifier.doi10.1021/ac0487597en_US
Appears in Collections:Scopus 2001-2005

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