| Literature DB >> 30137694 |
Oleta T Johnson1, Tanpreet Kaur2, Amanda L Garner1,2.
Abstract
Proteins containing intrinsic disorder often form secondary structure upon interaction with a binding partner. Modulating such structures presents an approach for manipulating the resultant functional outcomes. Translational repressor protein 4E-BP1 is an example of an intrinsically disordered protein that forms an α-helix upon binding to its protein ligand, eIF4E. Current biophysical methods for analyzing binding-induced structural changes are low-throughput, require large amounts of sample, or are extremely sensitive to signal interference by the ligand itself. Herein, we describe the discovery and development of a conditionally fluorescent 4E-BP1 peptide that reports structural changes of its helix in high-throughput format. This reporter peptide is based on conditional quenching of fluorescein by thioamides. In this case, fluorescence signal increases as the peptide becomes more ordered. Conversely, destabilization of the α-helix results in decreased fluorescence signal. The low concentration and low volume of peptide required make this approach amenable for high-throughput screening to discover ligands that alter peptide secondary structure.Entities:
Keywords: bioorganic chemistry; fluorescent probes; helical structures; high-throughput screening; protein folding
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Year: 2018 PMID: 30137694 PMCID: PMC6482830 DOI: 10.1002/cbic.201800377
Source DB: PubMed Journal: Chembiochem ISSN: 1439-4227 Impact factor: 3.164