Rapid characterization of folding and binding interactions with thermolabile ligands by DSC

dc.contributor.authorHarkness V, Robert W
dc.contributor.authorSlavkovic, Sladjana
dc.contributor.authorJohnson, Philip E.
dc.contributor.authorMittermaier, Anthony K.
dc.date.accessioned2023-05-10T17:13:55Z
dc.date.available2023-05-10T17:13:55Z
dc.date.issued2016-10-23
dc.description.abstractDifferential scanning calorimetry (DSC) is a powerful technique for measuring tight biomolecular interactions. However, many pharma- ceutically relevant ligands are chemically unstable at the high temperatures used in DSC analyses. Thus, measuring binding inter- actions is challenging because the concentrations of ligands and thermally-converted products are constantly changing within the calorimeter cell. Using experimental data for two DNA aptamers that bind to the thermolabile ligand cocaine, we present a new global fitting analysis that yields the complete set of folding and binding parameters for the initial and final forms of the ligand from a pair of DSC experiments, while accounting for the thermal conversion. Furthermore, we show that the rate constant for thermolabile ligand conversion may be obtained with only one additional DSC dataset.en_US
dc.identifier.citationChem. Commun. 52 (2016): 13471--13474en_US
dc.identifier.urihttps://doi.org/10.1039/c6cc05576aen_US
dc.identifier.urihttp://hdl.handle.net/10315/41140
dc.language.isoenen_US
dc.publisherThe Royal Society of Chemistryen_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titleRapid characterization of folding and binding interactions with thermolabile ligands by DSCen_US
dc.typeArticleen_US

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