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Further studies into the Boc/solid-phase synthesis of Ser(P)- and Thr(P)-containing peptides.

作者信息

Perich J W, Terzi E, Carnazzi E, Seyer R, Trifilieff E

机构信息

Centre of Pharmacology-Endocrinology, CNRS-INSERM, Montpellier, France.

出版信息

Int J Pept Protein Res. 1994 Oct;44(4):305-12. doi: 10.1111/j.1399-3011.1994.tb01013.x.

Abstract

The Ser(P)-containing peptide corresponding to phospholamban 11-19, Ac-Ala-Ile-Arg-Arg-Ala-Ser(P)-Thr-Ile-Glu-NH2, was prepared by the use of Boc-Ser(PO3Ph2)-OH in Boc/solid-phase peptide synthesis followed by HF cleavage of the peptide from the polystyrene resin and subsequent platinum-mediated hydrogenolytic cleavage of the phenyl phosphate groups. A study of the HF deprotection step showed that extensive dephosphorylation of the Ser(PO3Ph2)-residue occurred using three commonly used HF conditions and gave rise to large quantities of the Ser-containing peptide. The subsequent study of model peptide systems under standard HF conditions established firstly that the extent of dephosphorylation was dependent on the HF-contact time, and secondly that the Ser(PO3Ph2) residue underwent dephosphorylation at a slightly higher rate than the Thr(PO3Ph2) residue.

摘要

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