Poly(hydroxyethyl methacrylate-co-methacrylamidoalanine) membranes and their utilization as metal-chelate affinity adsorbents for lysozyme adsorption


Garipcan B., Say R., Patir S., Arica Y., Denizli A.

JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, cilt.13, sa.5, ss.563-577, 2002 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 13 Sayı: 5
  • Basım Tarihi: 2002
  • Doi Numarası: 10.1163/15685620260178409
  • Dergi Adı: JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.563-577
  • Anahtar Kelimeler: lysozyme adsorption, amino acid membranes, poly(HEMA), metal chelates, ION AFFINITY, HUMAN-PLASMA, MICROFILTRATION MEMBRANES, PROTEIN ADSORPTION, CHROMATOGRAPHY, PURIFICATION, PERFORMANCE, PEPTIDES, BINDING, SURFACE
  • Anadolu Üniversitesi Adresli: Hayır

Özet

Different adsorbents have been reported in the literature for protein purification. The authors have developed a novel and new approach to obtain high protein adsorption capacity utilizing a 2-methacrylamidoalanine-containing membrane. Amino acid ligand 2-methacrylamidoalanine (MAAL) monomer was synthesized using methacryloyl chloride and alanine. Poly(2-hydroxyethylmethacrylate-co-2-methacrylamidoalanine) [p(HEMA-co-MAAL)] membranes were then prepared by UV-initiated photopolymerization of HEMA and MAAL in the presence of an initiator (azobisisobutyronitrile, AIBN). The synthesized MAAL monomer was characterized by NMR. p(HEMA-co-MAAL) membranes were characterized by swelling studies, porosimeter, SEM, FTIR, and elemental analysis. These membranes have macropores in the size range of 5-10 mum. Cu(II) ions (25.9 mmol/m(2)) were chelated on these membranes. p(HEMA-co-MAAL) membranes were used to study the adsorption of lysozyme from aqueous media containing different amounts of lysozyme (0.1-3.0 mg/l) and at different pH values (4.0-8.0). The non-specific adsorption of lysozyme on the pHEMA membranes was negligible (0.9 mug/cm(2)). Incorporation of MAAL increased the lysozyme adsorption significantly up to 2.96 mg/cm(2). The lysozyme adsorption capacity of the Cu(II) incorporated membranes (9.98 mg/cm(2)) was greater than that of the p(HEMA-co-MAAL) membranes. More than 90% of the adsorbed lysozyme was desorbed in I h in the desorption medium containing 1.0 M NaCl and 0.025 M EDTA. The metal-chelate affinity membranes are suitable for repeated use for more than ten cycles without a noticeable loss of capacity.