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PMID: 9452382 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Fluorescent, sequence-selective peptide detection by synthetic small molecules.

Science (New York, N.Y.) ·Vol. 279 ·No. 5352 ·1998-02-06 ·Pages 851-3

Chen CT, Wagner H, Still WC

Abstract

Small organic sensor molecules were prepared that bind and signal the presence of unlabeled tripeptides in a sequence-selective manner. Sequence-selective peptide binding is a difficult problem because small peptides are highly flexible and there are no clear rules for designing peptide-binding molecules as there are for the nucleic acids. The signaling system involved the application of fluorescence energy transfer and provided large, real-time fluorescence increases (300 to 500 percent) upon peptide binding. With it, these sensors were sensitive enough to detect unlabeled cognate peptides both in organic solution and in the solid state at low micromolar concentrations.

MeSH Terms
Binding Sites Energy Transfer Fluorescence Microspheres Oligopeptides/analysis,metabolism Peptide Library Peptides, Cyclic/chemical synthesis,chemistry,metabolism Polystyrenes Spectrometry, Fluorescence
Chemicals
Oligopeptides Peptide Library Peptides, Cyclic Polystyrenes chemosensor 1 chemosensor 2
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Chen C T
Department of Chemistry, Columbia University, New York, NY 10027, USA.
Wagner H
Still W C
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1998-02-06
Pages
851-3
Language
English
Region
United States
NLM ID
0404511
Subset
IM
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