Abstract
Mono- and di-substituted triazines were appended to the side chain of lysine or ornithine, which was then used in the synthesis of peptides. In this way, environment-sensitive reporter groups can be included in a sequence-specific manner in a peptide. The triazine adducts are stable to standard conditions employed in peptide synthesis. Several model peptides showing the utility of these conjugates were prepared
Keywords: triazine, peptides, aminochlorotriszines, fluorophores, ornithine
Protein & Peptide Letters
Title: Triazine Conjugates for Multiple Site-Specific Labeling of Peptides
Volume: 8 Issue: 2
Author(s): Jonathan A. Zerkowski and Douglas A. Schftner
Affiliation:
Keywords: triazine, peptides, aminochlorotriszines, fluorophores, ornithine
Abstract: Mono- and di-substituted triazines were appended to the side chain of lysine or ornithine, which was then used in the synthesis of peptides. In this way, environment-sensitive reporter groups can be included in a sequence-specific manner in a peptide. The triazine adducts are stable to standard conditions employed in peptide synthesis. Several model peptides showing the utility of these conjugates were prepared
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Cite this article as:
Zerkowski A. Jonathan and Schftner A. Douglas, Triazine Conjugates for Multiple Site-Specific Labeling of Peptides, Protein & Peptide Letters 2001; 8 (2) . https://dx.doi.org/10.2174/0929866013409562
DOI https://dx.doi.org/10.2174/0929866013409562 |
Print ISSN 0929-8665 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5305 |
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