Low molecular weight end-functionalized poly(N-vinylpyrrolidinone) for the modification of polypeptide aminogroups
Academic Article
Publication Date:
1994
Abstract:
New monofunctionalized amphiphilic oligomers, poly (N-vinyl
pyrrolidinones) with an hydroxyl end group, were prepared by radical
polymerization with 2-isopropoxyethanol, fractionated by both gel-permeation
chromatography and fractional precipitation. The terminal hydroxyl group oligomers
was activated and reacted with the amino groups of a model peptide, and a protein.
These hydroxylated oligomers were also converted to carboxylate end group which
were also activated and used as protein and peptide modifying agents.
New monofunctionalized amphiphilic oligomers, poly (N-vinyl pyrrolidionones) with
an hydroxyl end group, were prepared by radical polymerization with 2-
isopropoxyethanol, fractionated by both gel-permeation chromatography and
fractional precipitation. The terminal hydroxyl group oligomers was activated and
reacted with the amino groups of a model peptide, and a protein. These
hydroxylated oligomers were also converted to carboxylate end group which were
also activated and used as protein and peptide modifying agents.
pyrrolidinones) with an hydroxyl end group, were prepared by radical
polymerization with 2-isopropoxyethanol, fractionated by both gel-permeation
chromatography and fractional precipitation. The terminal hydroxyl group oligomers
was activated and reacted with the amino groups of a model peptide, and a protein.
These hydroxylated oligomers were also converted to carboxylate end group which
were also activated and used as protein and peptide modifying agents.
New monofunctionalized amphiphilic oligomers, poly (N-vinyl pyrrolidionones) with
an hydroxyl end group, were prepared by radical polymerization with 2-
isopropoxyethanol, fractionated by both gel-permeation chromatography and
fractional precipitation. The terminal hydroxyl group oligomers was activated and
reacted with the amino groups of a model peptide, and a protein. These
hydroxylated oligomers were also converted to carboxylate end group which were
also activated and used as protein and peptide modifying agents.
CRIS type:
1.1 Articolo in rivista
List of contributors:
Sartore, Luciana; E., Ranucci; P., Ferruti; P., Caliceti; O., Schiavon; F. M., Veronese
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