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The binding affinity and kinetics of target engagement are fundamental to establishing structure-activity relationships (SARs) for prospective therapeutic agents. Enhancing these binding parameters for operative targets, while minimizing binding to off-target sites, can translate to improved drug efficacy and a widened therapeutic window. Compound activity is typically assessed through modulation of an observed phenotype in cultured cells. Quantifying the corresponding binding properties under common cellular conditions can provide more meaningful interpretation of the cellular SAR analysis. Consequently, methods for assessing drug binding in living cells have advanced and are now integral to medicinal chemistry workflows. In this review, we survey key technological advancements that support quantitative assessments of target occupancy in cultured cells, emphasizing generalizable methodologies able to deliver analytical precision that heretofore required reductionist biochemical approaches.

Original publication

DOI

10.1146/annurev-biochem-011420-092302

Type

Journal article

Journal

Annu Rev Biochem

Publication Date

20/06/2020

Volume

89

Pages

557 - 581

Keywords

NanoBRET, SAR, chemical proteomics, energy transfer, structure–activity relationship, target engagement, target occupancy, Bioluminescence Resonance Energy Transfer Techniques, Cell Survival, Cells, Cultured, Chemistry, Pharmaceutical, Fluorescent Dyes, Genes, Reporter, High-Throughput Screening Assays, Humans, Kinetics, Molecular Probe Techniques, Molecular Targeted Therapy, Optical Imaging, Small Molecule Libraries, Structure-Activity Relationship