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Spot arrays on modified glass surfaces for efficient SPOT synthesis and on-chip bioassay of peptides

Authors
Kim, DHShin, DSLee, YS
Issue Date
Oct-2007
Publisher
JOHN WILEY & SONS LTD
Citation
JOURNAL OF PEPTIDE SCIENCE, v.13, no.10, pp 625 - 633
Pages
9
Journal Title
JOURNAL OF PEPTIDE SCIENCE
Volume
13
Number
10
Start Page
625
End Page
633
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/148350
DOI
10.1002/psc.884
ISSN
1075-2617
1099-1387
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 a-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.
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