Assessing reversible and irreversible binding effects of kinase covalent inhibitors through ADP-Glo assays

Typical enzymatic inhibition assays often demonstrate improved potency for kinase covalent inhibitors compared to reversible inhibitors. This can primarily be attributed to the irreversible mode of action and could affect the evaluations of the ATP-competitive nature of covalent inhibitors, hinderin...

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Veröffentlicht in:STAR protocols 2021-09, Vol.2 (3), p.100717-100717, Article 100717
Hauptverfasser: Schröder, Martin, Chaikuad, Apirat
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Sprache:eng
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Zusammenfassung:Typical enzymatic inhibition assays often demonstrate improved potency for kinase covalent inhibitors compared to reversible inhibitors. This can primarily be attributed to the irreversible mode of action and could affect the evaluations of the ATP-competitive nature of covalent inhibitors, hindering optimization of these compounds. Here, we describe a version of ADP-Glo assay, in which modification of inhibitor incubation time in the presence or absence of ATP enables a quick assessment of relative reversible and irreversible effects of kinase covalent inhibitors. For complete details on the use and execution of this protocol, please refer to Schröder et al. (2020). [Display omitted] •Simple enzymatic assays for quick assessment of kinase covalent inhibitors•Modification of incubation time allows probing ATP-competitive nature of inhibitors•The assays enable the evaluation of relative reversible and irreversible effects Typical enzymatic inhibition assays often demonstrate improved potency for kinase covalent inhibitors compared to reversible inhibitors. This can primarily be attributed to the irreversible mode of action and could affect the evaluations of the ATP-competitive nature of covalent inhibitors, hindering optimization of these compounds. Here, we describe a version of ADP-Glo assay, in which modification of inhibitor incubation time in the presence or absence of ATP enables a quick assessment of relative reversible and irreversible effects of kinase covalent inhibitors.
ISSN:2666-1667
2666-1667
DOI:10.1016/j.xpro.2021.100717