Versatile synthesis of fluorescent, cross-linked peptides as biological probes with the advantage of high helix content

Versatile synthesis of fluorescent, cross-linked peptides as biological probes with the advantage... A variety of fluorophores were introduced at the N-termini of short peptides for use as biological-probes. The fluorescent peptides were cross-linked with a diacetylenic cross-linking agent between the amino acid side chains of ornithine (Orn) residues to produce peptides with high helix content. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Research on Chemical Intermediates Springer Journals

Versatile synthesis of fluorescent, cross-linked peptides as biological probes with the advantage of high helix content

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Publisher
Springer Netherlands
Copyright
Copyright © 2012 by Springer Science+Business Media B.V.
Subject
Chemistry; Catalysis; Physical Chemistry; Inorganic Chemistry
ISSN
0922-6168
eISSN
1568-5675
D.O.I.
10.1007/s11164-012-0651-5
Publisher site
See Article on Publisher Site

Abstract

A variety of fluorophores were introduced at the N-termini of short peptides for use as biological-probes. The fluorescent peptides were cross-linked with a diacetylenic cross-linking agent between the amino acid side chains of ornithine (Orn) residues to produce peptides with high helix content.

Journal

Research on Chemical IntermediatesSpringer Journals

Published: Jul 3, 2012

References

  • Chemical biology: a Notch above other inhibitors
    Arora, PS; Ansari, AZ
  • Fluorescent organophosphonates as inhibitors of microbial lipases
    Oskolkova, OV; Saf, R; Zenzmaier, E; Hermetter, A

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