Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1367084 | Bioorganic & Medicinal Chemistry Letters | 2007 | 5 Pages |
In this paper, we describe an application of 202-membered fluorescently labeled peptide library designed to take an α-helix secondary structure. As a proof-of-concept experiment, a calmodulin (CaM)/calcineurin (Cn) pair was chosen to screen α-helical peptide ligands that tightly bind to CaM and also control enzymatic functions of Cn. Three peptides were successfully selected from the library by assaying Cn-phosphatase activities and peptide–CaM interactions (dual check process). The strategy using a designed peptide library shows real promise as a peptide-based high-throughput screening system.
Graphical abstractDemonstrated was the application of screening for peptide ligands that tightly bind to a target protein and also control the protein’s functions. The strategy using a designed peptide library shows real promise as a peptide-based novel screening system.Figure optionsDownload full-size imageDownload as PowerPoint slide