Gelatin-Immobilised Poly(hydroxyethyl methacrylate) Cryogel for Affinity Purification of Fibronectin


Percin I., Aksoz E., DENİZLİ A.

APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY, cilt.171, sa.2, ss.352-365, 2013 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 171 Sayı: 2
  • Basım Tarihi: 2013
  • Doi Numarası: 10.1007/s12010-013-0352-6
  • Dergi Adı: APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.352-365
  • Anahtar Kelimeler: Fibronectin purification, Human plasma, Monolithic column, Cryogel, Gelatin, PHEMA, HUMAN-PLASMA FIBRONECTIN, MONOLITHIC CRYOGELS, CHOLESTEROL REMOVAL, CHROMATOGRAPHY, SEPARATION, COMPOSITE, MEMBRANES, PROTEINS, BINDING
  • Hacettepe Üniversitesi Adresli: Evet

Özet

In this work, fibronectin purification from human plasma with the gelatin-immobilised poly(hydroxyethyl methacrylate) (PHEMA) cryogel has been evaluated. The PHEMA cryogel was prepared by cryo-polymerisation which proceeds in an aqueous solution of monomer frozen inside a plastic syringe. The PHEMA cryogel contained interconnected macrochannels of 10-200 mu m in diameter. Gelatin molecules were covalently immobilised onto the PHEMA cryogel via carbodiimide activation. The gelatin-immobilised PHEMA cryogel was used to purify fibronectin from human plasma. Fibronectin adsorption from human plasma on the PHEMA cryogel was 0.30 mg/ml, while much higher adsorption values, up to 38 mg/ml, was obtained with the gelatin-immobilised PHEMA cryogel. The fibronectin adsorption capacity of the gelatin-immobilised PHEMA cryogel did not change with an increase in the flow rate of plasma. Up to 92 % of the adsorbed fibronectin was eluted using 2 M urea containing 1 M NaCl as elution agent. The adsorption-elution cycle was repeated ten times using the same PHEMA cryogel. No remarkable decrease was detected in the adsorption capacity of the gelatin-immobilised PHEMA cryogel.