Highly selective cleavage of pyroglutamyl-peptide bond in concentrated hydrochloric acid.

Abstract:

:Highly selective cleavage reaction of pGlu-peptide bond is described. Two model peptides, pGlu-X-Ala-Phe-OH (X = Ile and Ser), and dog neuromedin U-8 (d-NMU-8) (1-7)-OH (pGlu-Phe-Leu-Phe-Arg-Pro-Arg-OH) were hydrolyzed in concentrated HCl at 0 degree C for from 6 days to 6 weeks to give the predominant cleavage products of pGlu-X linkage of pGlu-X-Ala-Phe-OH and the pGlu-Phe linkage of d-NMU-8 (1-7)-OH, respectively. The ring-opening reaction of the pyrrolidone moiety of the pGlu residue occurred to a considerably lesser extent.

authors

Hashimoto T,Saito S,Ohki K,Sakura N

doi

10.1248/cpb.44.877

subject

Has Abstract

pub_date

1996-04-01 00:00:00

pages

877-9

issue

4

eissn

0009-2363

issn

1347-5223

journal_volume

44

pub_type

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