Quantitative analyses of aggregation, autofluorescence, and reactivity artifacts in a screen for inhibitors of a thiol protease.

Paradigms and Technologies
Medicinal Chemistry

Abstract

The perceived and actual burden of false positives in high-throughput screening has received considerable attention; however, few studies exist on the contributions of distinct mechanisms of nonspecific effects like chemical reactivity, assay signal interference, and colloidal aggregation. Here, we analyze the outcome of a screen of 197861 diverse compounds in a concentration-response format against the cysteine protease cruzain, a target expected to be particularly sensitive to reactive compounds, and using an assay format with light detection in the short-wavelength region where significant compound autofluorescence is typically encountered. Approximately 1.9% of all compounds screened were detergent-sensitive inhibitors. The contribution from autofluorescence and compounds bearing reactive functionalities was dramatically lower: of all hits, only 1.8% were autofluorescent and 1.5% contained reactive or undesired functional groups. The distribution of false positives was relatively constant across library sources. The simple step of including detergent in the assay buffer suppressed the nonspecific effect of approximately 93% of the original hits.

Authors

Jadhav, Ajit; Ferreira, Rafaela S; Klumpp-Thomas, Carleen; Mott, Bryan T; Austin, Christopher; Inglese, James; Thomas, Craig; Maloney, David J; Shoichet, Brian K; Simeonov, Anton;

Keywords

  • Artifacts
  • Bacterial Proteins/ antagonists & inhibitors
  • Cysteine Endopeptidases
  • Cysteine Proteinase Inhibitors/ analysis
  • Cysteine Proteinase Inhibitors/ chemistry
  • Cysteine Proteinase Inhibitors/ pharmacology
  • Detergents/ pharmacology
  • Drug Evaluation, Preclinical/ methods
  • Fluorescence
  • High-Throughput Screening Assays/ methods
  • Protozoan Proteins/ antagonists & inhibitors
  • Structure-Activity Relationship
  • beta-Lactamase Inhibitors
  • beta-Lactamases

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