| Literature DB >> 17694567 |
Do-Hyun Kim1, Dong-Sik Shin, Yoon-Sik Lee.
Abstract
To make SPOT synthesis of peptides and their assays on glass surfaces more convenient, a simple method for making spot arrays on a slide glass was designed through patterning with a photoresist and perfluorination followed by amination with various silane compounds and polymers. With these spot-arrayed glass surfaces, we could measure the coupling completion of each Fmoc amino acid on the glass surface by direct fluorescence analysis after fluorescence-labeling the amino groups on the surface of each spot. Then we synthesized several types of decapeptides and HPQ-pentapeptides on the spot-arrayed glasses and identified the optimal surface condition for stepwise peptide coupling and on-chip bioassay. After optimizing the surface conditions, we synthesized a model library of biotin-Gly-Ala-P(1)-Gly (P(1): one of 19 amino acids) and successfully replicated the well-known alpha-chymotrypsin subsite specificities through Cy5-streptavidin binding to the remaining biotin on the surface after the enzymatic digestion. Copyright (c) 2007 European Peptide Society and John Wiley & Sons, Ltd.Entities:
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Year: 2007 PMID: 17694567 DOI: 10.1002/psc.884
Source DB: PubMed Journal: J Pept Sci ISSN: 1075-2617 Impact factor: 1.905