Article ID Journal Published Year Pages File Type
1367084 Bioorganic & Medicinal Chemistry Letters 2007 5 Pages PDF
Abstract

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

Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
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