Solid-phase synthesis of an Htc-containingdimer analog of the autophosphorylationsite of pp60src PTK: Effective acylationconditions for Htc residues |
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Authors: | Paolo Ruzza Andrea Calderan Franco Cavaggion Gianfranco Borin |
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Affiliation: | (1) C.N.R.-Centro di Studio sui Biopolimeri, c/o Dipartimento di Chimica Organica, Università di Padova, via Marzolo 1, I-35131 Padova, Italy |
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Abstract: | Summary The difficulty during SPPS in acylating the secondary amino group of Htc, a locally constrained tyrosine, can be correlated with the steric hindrance of the amino acid or with the conformation of the growing peptide chain. Our experimental data indicate that the availability of the Htc amino group is associated with its steric hindrance rather than a conformational effect of the peptide chain. An optimized solid phase automated protocol for Htc is reported. Under optimal conditions, Fmoc-amino acids with hindered side chains were incorporated in approximately 99% yield using HATU as coupling reagent. Unhindered side chain amino acid acylated the secondary amino group of Htc in good yield under classical HBTU/HOBt coupling conditions. Abbreviations: Abbreviations used for amino acids and the designation of peptides follow the rules of the IUPAC-IUB Commission of Biochemical Nomenclature [J. Biol. Chem., 247 (1972) 977–983]. Amino acid symbols denote thel-configuration where applicable, unless indicated otherwise. The following additional, abbreviations are used |
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Keywords: | coupling reagents HATU hindered amino acids solid phase |
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