L-histidine imprinted synthetic receptor for biochromatography applications


Oezcan A. A. , Say R., Denizli A., Ersoez A.

ANALYTICAL CHEMISTRY, vol.78, no.20, pp.7253-7258, 2006 (SCI-Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 78 Issue: 20
  • Publication Date: 2006
  • Doi Number: 10.1021/ac060536o
  • Journal Name: ANALYTICAL CHEMISTRY
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.7253-7258
  • Hacettepe University Affiliated: Yes

Abstract

We have proposed novel surface-imprinted beads for selective separation of cytochrome c (cyt c) by N-methacryloyl(L)-histidine-copper(II) [MAH-Cu(II)] as a new metal-chelating monomer via metal coordination interactions and histidine template. We have combined molecular imprinting with the ability of histidine to chelate metal ions to create ligand exchange beads suitable for the binding of cyt c (surface histidine exposed protein). The histidine imprinted beads were produced by suspension polymerization of MAH-Cu(II)-L-histidine and ethylene glycol dimethacrylate. After polymerization, the template (L-histidine) was removed from the beads using methanolic KOH, thus getting histidine imprinted metal-chelate beads. L-Histidine imprinted metal-chelate beads can be used several times without considerable loss of cyt c adsorption capacity. The association constant (K-a) for the specific interaction between the template imprinted polymer and the template (L-histidine) itself were determined by Scatchard plots using L-histidine imprinted beads and found as 58 300 M-1. Finally, we have used these histidine imprinted beads for cyt c and ribonuclease A ( surface histidine exposed proteins) and enantiometric separation of D- and L-histidine by FPLC.