Premium
On the amino‐acid‐sequence distribution in benzylglutamate‐methionine copolymers prepared from N ‐carboxyanhydrides
Author(s) -
Hill D. J. T.,
Cardinaux F.,
Scheraga H. A.
Publication year - 1977
Publication title -
biopolymers
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.556
H-Index - 125
eISSN - 1097-0282
pISSN - 0006-3525
DOI - 10.1002/bip.1977.360161110
Subject(s) - cyanogen bromide , chemistry , methionine , copolymer , homoserine , glutamic acid , polymer , amino acid , sequence (biology) , polymer chemistry , polymerization , organic chemistry , peptide sequence , biochemistry , quorum sensing , virulence , gene
The amino‐acid‐sequence distribution in poly(γ‐benzyl‐ L ‐glutamate, L ‐methionine) prepared by polymerization of the respective N ‐carboxyanhydrides has been investigated. This copolymer was converted first to poly( L ‐glutamic acid, L ‐methionine), which was subsequently cleaved by treatment with cyanogen bromide. The resulting material was fractionated into oligomers of (glutamic acid) n ‐homoserine whose relative molar amounts were determined quantitatively. The results have been compared with those for a random incorporation of the methionine in a γ‐benzylglutamate host polymer. Fairly close agreement has been found.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom