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Synthesis and screening of a combinatorial peptide library for ligands to target transferrin: Miniaturizing the library

Posted on:2011-10-02Degree:M.SType:Thesis
University:University of North TexasCandidate:Brown, Jennifer MFull Text:PDF
GTID:2444390002455201Subject:Chemistry
Abstract/Summary:PDF Full Text Request
Combinatorial libraries are used in the search for ligands that bind to target proteins. Fmoc solid-phase peptide synthesis is routinely used to generate such libraries. Microwave-assisted peptide synthesis was employed here to decrease reaction times by 80-90%. Two One-Bead-One-Compound combinatorial libraries were synthesized on 130mum beads (one containing 750 members and the other 16, 807). The use of smaller solid supports would have many important practical advantages including; increased library diversity per unit mass, smaller quantities of library needed to generate hits, and screening could be conducted by using a standard flow cytometer. To this end, a miniaturized peptide library was synthesized on 20 mum beads to demonstrate proof of principle.;A small sample from the 16,807-member library was screened against transferrin-AlexaFluro 647, a protein responsible for iron transport in vivo. A number of hits were identified and sequenced using techniques coupling nanomanipulation with nanoelectrospray mass spectrometry.
Keywords/Search Tags:Peptide, Synthesis, Library
PDF Full Text Request
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