2019
DOI: 10.1111/bph.14841
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Considerations for improved performance of competition association assays analysed with the Motulsky–Mahan's “kinetics of competitive binding” model

Abstract: Background and Purpose: Target engagement dynamics can influence drugs' pharmacological effects. Kinetic parameters for drug:target interactions are often quantified by evaluating competition association experiments-measuring simultaneous protein binding of labelled tracers and unlabelled test compounds over time-with Motulsky-Mahan's "kinetics of competitive binding" model. Despite recent technical improvements, the current assay formats impose practical limitations to this approach. This study aims at the ch… Show more

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Cited by 13 publications
(14 citation statements)
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“…In a corresponding ensemble-based ISA experiment, the temporal evolution of the net change in TDC occupancy ( ) at > inh is given by 26,38 ( and where TDC is the concentration of suspended TDC. Although Eq.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…In a corresponding ensemble-based ISA experiment, the temporal evolution of the net change in TDC occupancy ( ) at > inh is given by 26,38 ( and where TDC is the concentration of suspended TDC. Although Eq.…”
Section: Resultsmentioning
confidence: 99%
“…radioactive labelling or fluorescence resonance energy transfer 26 . Nonetheless, as repeatedly shown, [27][28][29] the kinetic window in terms of on and off values that can be quantified is strictly restricted by the kinetic profile of the TDC in relation to that of the screening compound. Further, if the TDC is instead immobilized on a surface with the competition measured using SPR, BLI, or OWG, only d can be determined and TDC has to have a very slow dissociation rate in such studies 30,31 .…”
Section: Introductionmentioning
confidence: 98%
“…7,52,53 It should noted that while measuring the rate constants is an effective way to measure affinity, kinetic binding assays require significant resources for assay development and data analysis. [59][60][61]…”
Section: Managing Equilibration Artifacts In Drug Discoverymentioning
confidence: 99%
“…A biosensor-based approach has recently been reported 11 , addressing this limitation but specific system customizations are required to enable routine application. Probe-based kinetic competition assays 12 may be implemented using surface plasmon resonance (SPR)-based biosensors 13 , or other equivalent flow-injection-based biosensors such as grating coupled interfereometry 14 . However, the estimation of transient kinetics and extremely rapid association processes (i.e.…”
Section: Introductionmentioning
confidence: 99%