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Solid-phase synthesis of C-terminal modified peptides

โœ Scribed by Jordi Alsina; Fernando Albericio


Publisher
Wiley (John Wiley & Sons)
Year
2003
Tongue
English
Weight
329 KB
Volume
71
Category
Article
ISSN
0006-3525

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โœฆ Synopsis


Abstract

Solidโ€phase synthesis of biomolecules, of which peptides are the principal example, is well established. However, synthetic peptides containing modifications at the carboxy termini are often desired because of their potential therapeutic properties. As a result, there is a necessity for effective solidโ€phase strategies for the preparation of peptides with Cโ€terminal end groups other than the usual carboxylic acid and carboxamide functionalities. The present article primarily reviews literature reports on methods for solidโ€phase synthesis of Cโ€terminal modified peptides. In addition, general information about biological activities and/or synthetic applications of each individual class of peptide is also provided. ยฉ 2003 Wiley Periodicals, Inc. Biopolymers (Pept Sci) 71: 454โ€“477, 2003


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## Abstract Many naturally occurring peptide acids, e.g., somatostatins, conotoxins, and defensins, contain a cysteine residue at the Cโ€terminus. Furthermore, installation of Cโ€terminal cysteine onto epitopic peptide sequences as a preliminary to conjugating such structures to carrier proteins is a