Nm. Obriensimpson et al., POLYMERIZATION OF UNPROTECTED SYNTHETIC PEPTIDES - A VIEW TOWARD SYNTHETIC PEPTIDE VACCINES, Journal of the American Chemical Society, 119(6), 1997, pp. 1183-1188
A generic method is reported for the assembly of multi-peptide polymer
s in which peptides are synthesized in the solid phase, the N-terminal
residue acryloylated, and the derivitized peptides cleaved, purified
and finally polymerized by free radical induced polymerization. The hi
gh molecular weight polymers generated in this way have individual pep
tides pendant from a backbone support. Incorporation of 6-aminohexanoy
l or other residue(s) at the N-terminus of the peptide prior to acrylo
ylation allows the peptide to be distanced from the polymer backbone a
nd incorporation of acryloylated reagents into the polymerization mixt
ure also permits distancing of pendant peptides along the length of th
e backbone support. The polymerization process results in highly antig
enic artificial proteins as measured by ELISA. Because this approach a
llows the incorporation of the same or combinations of different purif
ied peptides into polymers, it lends itself to the assembly of potenti
al vaccine candidates containing epitopes from single or multiple path
ogens into a single covalent structure.