Abstract
C-terminal peptide α-thioesters are valuable intermediates in the synthesis/semisynthesis of proteins by native chemical ligation. They are prepared either by solid-phase peptide synthesis (SPPS) or biosynthetically by protein splicing techniques. The present paper reviews the different methods available for the chemical synthesis of peptide α-thioesters using Fmoc-based SPPS.
Keywords: chemical protein synthesis, native chemical ligation, peptide thioester, hydrazine linker, protein engineering, fmoc-chemistry
Protein & Peptide Letters
Title: Synthesis of Proteins by Native Chemical Ligation Using Fmoc-Based Chemistry
Volume: 12 Issue: 8
Author(s): Julio A. Camarero and Alexander R. Mitchell
Affiliation:
Keywords: chemical protein synthesis, native chemical ligation, peptide thioester, hydrazine linker, protein engineering, fmoc-chemistry
Abstract: C-terminal peptide α-thioesters are valuable intermediates in the synthesis/semisynthesis of proteins by native chemical ligation. They are prepared either by solid-phase peptide synthesis (SPPS) or biosynthetically by protein splicing techniques. The present paper reviews the different methods available for the chemical synthesis of peptide α-thioesters using Fmoc-based SPPS.
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Cite this article as:
Camarero A. Julio and Mitchell R. Alexander, Synthesis of Proteins by Native Chemical Ligation Using Fmoc-Based Chemistry, Protein & Peptide Letters 2005; 12 (8) . https://dx.doi.org/10.2174/0929866054864166
DOI https://dx.doi.org/10.2174/0929866054864166 |
Print ISSN 0929-8665 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5305 |
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