Confirming Target Engagement for Reversible Inhibitors in Vivo by Kinetically Tuned Activity-Based Probes

• Published in: Journal of the American Chemical Society Vol. 134; no. 25; pp. 10345 - 10348
• Main Authors: Adibekian, Alexander, Martin, Brent R, Chang, Jae Won, Hsu, Ku-Lung, Tsuboi, Katsunori, Bachovchin, Daniel A, Speers, Anna E, Brown, Steven J, Spicer, Timothy, Fernandez-Vega, Virneliz, Ferguson, Jill, Hodder, Peter S, Rosen, Hugh, Cravatt, Benjamin F
• Format: Journal Article
• Language: English
• Published: WASHINGTON American Chemical Society 27.06.2012; Amer Chemical Soc
• Subjects: Amides - chemistry; Animals; Binding, Competitive; Cells, Cultured; Chemistry; Chemistry, Multidisciplinary; Drug Delivery Systems; Enzyme Inhibitors - chemistry; Enzyme Inhibitors - pharmacology; Mice; Molecular Structure; Physical Sciences; Piperidines - chemistry; Protein Binding - drug effects; Science & Technology; Small Molecule Libraries - chemistry; Small Molecule Libraries - pharmacology; Structure-Activity Relationship; LYSOPHOSPHOLIPASE; CHEMISTRY; ACYL-PROTEIN THIOESTERASE-1; IDENTIFICATION; DRUG DISCOVERY
• ISSN: 0002-7863; 1520-5126
• DOI: 10.1021/ja303400u

The development of small-molecule inhibitors for perturbing enzyme function requires assays to confirm that the inhibitors interact with their enzymatic targets in vivo. Determining target engagement in vivo can be particularly challenging for poorly characterized enzymes that lack known biomarkers (e.g., endogenous substrates and products) to report on their inhibition. Here, we describe a competitive activity-based protein profiling (ABPP) method for measuring the binding of reversible inhibitors to enzymes in animal models. Key to the success of this approach is the use of activity-based probes that show tempered rates of reactivity with enzymes, such that competition for target engagement with reversible inhibitors can be measured in vivo. We apply the competitive ABPP strategy to evaluate a newly described class of piperazine amide reversible inhibitors for the serine hydrolases LYPLA1 and LYPLA2, two enzymes for which selective, in vivo active inhibitors are lacking. Competitive ABPP identified individual piperazine amides that selectively inhibit LYPLA1 or LYPLA2 in mice. In summary, competitive ABPP adapted to operate with moderately reactive probes can assess the target engagement of reversible inhibitors in animal models to facilitate the discovery of small-molecule probes for characterizing enzyme function in vivo.