| Literature DB >> 17602682 |
Fujie Tanaka1, Roberta Fuller, Lily Asawapornmongkol, Axel Warsinke, Sarah Gobuty, Carlos F Barbas.
Abstract
A 21-mer peptide that can be used to covalently introduce synthetic molecules into proteins has been developed. Phage-displayed peptide libraries were subjected to reaction-based selection with 1,3-diketones. The peptide was further evolved by addition of a randomized region and reselection for improved binding. The resulting 21-mer peptide had a reactive amino group that formed an enaminone with 1,3-diketone and was used as a tag for labeling of maltose binding protein. Using this peptide tag and 1,3-diketone derivatives, a variety of molecules such as reporter probes and functionalities may be covalently introduced into proteins of interest.Entities:
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Year: 2007 PMID: 17602682 PMCID: PMC2518172 DOI: 10.1021/bc070080x
Source DB: PubMed Journal: Bioconjug Chem ISSN: 1043-1802 Impact factor: 4.774