Nanomolar binding affinity of quinine-based antimalarial compounds by the cocaine-binding aptamer

dc.contributor.authorSlavkovic, Sladjana
dc.contributor.authorChurcher, Zachary R
dc.contributor.authorJohnson, Philip E
dc.date.accessioned2023-05-10T16:28:07Z
dc.date.available2023-05-10T16:28:07Z
dc.date.issued2018-09-17
dc.description.abstractAn unusual feature of the cocaine-binding aptamer is that it binds quinine much tighter than the ligand it was selected for, cocaine. Here we expand the repertoire of ligands that this aptamer binds to include the quinine- based antimalarial compounds amodiaquine, mefloquine, chloroquine and primaquine. Using isothermal titra- tion calorimetry (ITC) we show that amodiaquine is bound by the cocaine-binding aptamer with an affinity of (7 ± 4) nM, one of the tightest aptamer-small molecule affinities currently known. Amodiaquine, mefloquine and chloroquine binding are driven by both a favorable entropy and enthalpy of binding, while primaquine, quinine and cocaine binding are enthalpy driven with unfavorable binding entropy. Using nuclear magnetic resonance (NMR) and ITC methods we show that these ligands compete for the same binding sites in the ap- tamer. Our identification of such a tight binding ligand for this aptamer should prove useful in developing new biosensor techniques and applications using the cocaine-binding aptamer as a model system.en_US
dc.identifier.citationBioorganic & Medicinal Chemistry 26 (2018): 5427–5434en_US
dc.identifier.urihttps://doi.org/10.1016/j.bmc.2018.09.017en_US
dc.identifier.urihttp://hdl.handle.net/10315/41135
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectAptamer; Isothermal titration calorimetry; NMR spectroscopy; Biomolecular interactionsen_US
dc.titleNanomolar binding affinity of quinine-based antimalarial compounds by the cocaine-binding aptameren_US
dc.typeArticleen_US

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