A high-throughput fluorescence chemical denaturation assay as a general screen for protein-ligand binding

Anal Biochem. 2011 Apr 1;411(1):155-7. doi: 10.1016/j.ab.2010.12.001. Epub 2010 Dec 5.

Abstract

Chemical denaturation of ligand-protein complexes can provide the basis of a label-free binding assay. Here, we show how the technique can be used as a sensitive/affordable screen of potential ligands from a pool of lead drug variants. To demonstrate, we characterized the binding of polyketide ligands based on the mTOR inhibitor rapamycin to the cellular immunophilin FKBP12. This used the intrinsic fluorescence of the protein to monitor the chemical denaturation of each FKBP12-ligand complex. The assay was then successfully modified to a 96-well plate-based screen. Both formats were able to differentiate binding affinities across a wide dynamic range.

MeSH terms

  • Fluorescence
  • Fluorometry
  • High-Throughput Screening Assays / methods*
  • Ligands
  • Protein Binding
  • Protein Denaturation*
  • Sirolimus / chemistry
  • Sirolimus / metabolism
  • Tacrolimus Binding Protein 1A / chemistry
  • Tacrolimus Binding Protein 1A / metabolism
  • Thermodynamics

Substances

  • Ligands
  • Tacrolimus Binding Protein 1A
  • Sirolimus