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Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/22516
Title: Synthesis of peptide sequences related to thrombospondin: factors affecting aspartimide by-product formation
Authors: Cebrián, Just; Domingo, Víctor M.; Reig Isart, Francesca
Keywords: Adhesion
Peptide synthesis
Issue Date: 19-Nov-2003
Publisher: Wiley-Blackwell
Citation: Journal of Peptide Research 62(6): 238-244 (2003)
Abstract: Aspartimide formation is one of the most common secondary reactions on solid phase peptide synthesis. In the present work, we describe the optimization of the synthesis of two thrombospondin fragments containing an Asp-Gly sequence that show a strong tendency to form cyclic aspartimide derivatives in an unusual high percentage. Several different strategies were applied changing type of resin, Fmoc-deprotection reagents, coupling additives, resin cleavage cocktails and the use of Hmb-Gly derivative to minimize the extension of this byproduct. Best results were obtained with cross-linked ethoxylate acrylate (CLEAR®-cross-linked ethoxylate Acrylate Resin)-type resin and pip/dimethylformamide deprotection. Besides, as in biological assays the aspartimide containing sequence resulted to be more active than the linear one, the optimization of its synthesis was also carried out.
Description: 7 pages, 3 figures, 1 table.-- PMID: 14632926 [PubMed].-- Printed version published Dec 2003
Publisher version (URL): http://dx.doi.org/10.1046/j.1399-3011.2003.00093.x
URI: http://hdl.handle.net/10261/22516
ISSN: 1397-002X (Print)
1399-3011 (Online)
DOI: 10.1046/j.1399-3011.2003.00093.x
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