ABSTRACT
A derivatization of cellulose was investigated for gaining up the solubility for subsequent conjugation reaction. N(ß)-Boc-ß-Ala, was introduced to the parent cellulose using carbonyl diimidazole. Degree of substitution towards the cellulose hydroxyls was 49%. Subsequent removal of Boc in trifluoroacetic acid (TFA) yielded ß-Ala-cellulose·TFA salt. A protected hexapeptide, Boc-Ser(Bzl)-Gly-Tyr(Bzl)-Ser(Bzl)-Gly-Lys(Z) was synthesized via 9 steps of peptide elongation, and the C-end carboxyl groups of the peptide was coupled with the ß-Ala-cellulose in a homogenous dimethyl sulfoxide solution, using 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide monohydrochloride to ensure the N(ß)-selective acylation. The degree of substitution of the protected peptide towards the ß-amino groups of ß-Ala-cellulose (DS%(/NH(2))) was 52% for 1.0 eq.mol of the protected peptide feed, and in the presence of N-hydroxysuccinimide, DS%(/NH(2)) was increased to 61%. At 4.0 eq.mol feed, almost quantitative conjugation was observed as DS%(/NH(2))=98-99%. Deprotection of the conjugate using thioanisole-TFA resulted in complete removal of Boc, Bzl on Tyr, and Z on Lys, while a very trace amount of Bzl on Ser seemed to be left uncleaved.
