One-step affinity purification of fetuin from fetal bovine serum

被引:35
|
作者
Cartellieri, S
Hamer, O
Helmholz, H
Niemeyer, B
机构
[1] GKSS Natl Res Ctr, Inst Coastal Res Phys & Chem Anal, D-21502 Geesthacht, Germany
[2] Univ Fed Armed Forces Hamburg, Inst Thermodynam, D-22043 Hamburg, Germany
关键词
affinity adsorbent; affinity separation; lectin; polymer; silica;
D O I
10.1042/BA20010067
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Fetuin is a plasma glycoprotein widely distributed in mammals. It has been used as a model protein for structural analyses and investigations into the biological properties of glycoproteins. A convenient one-step procedure for biospecific isolation of fetuin from fetal bovine serum was developed on the basis of wheatgerm agglutinin (WGA) affinity separation. Two different porous supports, a silica-based material and a polymer-based material, were used for the immobilization of WGA. The prepared WGA adsorbents were characterized and process parameters of the affinity separation of fetuin were investigated and optimized. WGA was immobilized on silica and polymer supports with coupling yields of 99.6 and 99.4% respectively and amounts of coupled ligand of 7.9 and 9.2 mg of WGA/ml respectively. It has been shown that the specific capacities for fetuin were 5.1 mg/ml on WGA-silica, 1.8 mg/ml on WGA-polymer and 4.1 mg/ml on WGA-agarose. All three adsorbents proved to be suitable for the biospecific separation of fetuin. The polymer-based WGA adsorbent was successfully applied in the purification of fetuin from fetal bovine serum in a one-step separation process. The identity and purity of the isolated product was verified by SDS/PAGE. Under optimized conditions up to 21.6 mg of fetuin could be isolated from I ml of serum. The procedure described was designed to be easily scaled-up for the production of fetuin.
引用
收藏
页码:83 / 89
页数:7
相关论文
共 50 条
  • [1] One-step purification of lactoperoxidase from bovine milk by affinity chromatography
    Atasever, Ali
    Ozdemir, Hasan
    Gulcin, Ilhami
    Kufrevioglu, O. Irfan
    FOOD CHEMISTRY, 2013, 136 (02) : 864 - 870
  • [2] One-step lactoferrin purification from bovine whey and colostrum by affinity membrane chromatography
    Wolman, F. J.
    Gonzalez Maglio, D.
    Grasselli, A.
    Cascone, O.
    JOURNAL OF MEMBRANE SCIENCE, 2007, 288 (1-2) : 132 - 138
  • [3] ONE-STEP AFFINITY PURIFICATION OF UREASE FROM JACK BEANS
    MENDES, MJ
    KARMALI, A
    BROWN, P
    BIOCHIMIE, 1988, 70 (10) : 1369 - 1371
  • [4] One-step purification of cholinesterase from human serum by CCC
    Shibusawa, Y
    Hosojima, T
    Nakata, M
    Shindo, H
    Ito, Y
    JOURNAL OF LIQUID CHROMATOGRAPHY & RELATED TECHNOLOGIES, 2001, 24 (11-12) : 1733 - 1744
  • [5] One-step affinity purification protocol for human telomerase
    Schnapp, G
    Rodi, HP
    Rettig, WJ
    Schnapp, A
    Damm, K
    NUCLEIC ACIDS RESEARCH, 1998, 26 (13) : 3311 - 3313
  • [6] One-step purification of glucoamylase by affinity precipitation with alginate
    Teotia, S
    Lata, R
    Khare, SK
    Gupta, MN
    JOURNAL OF MOLECULAR RECOGNITION, 2001, 14 (05) : 295 - 299
  • [7] ONE-STEP PURIFICATION OF BOVINE ADRENAL GLUCOSE-6-PHOSPHATE-DEHYDROGENASE BY AFFINITY CHROMATOGRAPHY
    BURGISSER, E
    FAUCHERE, JL
    HELVETICA CHIMICA ACTA, 1976, 59 (03) : 760 - 765
  • [8] ONE-STEP PURIFICATION PROCEDURE OF ELASTASE FROM PANCREATIC POWDER BY AFFINITY CHROMATOGRAPHY
    KATAGIRI, K
    TAKEUCHI, T
    TANIGUCHI, K
    SASAKI, M
    ANALYTICAL BIOCHEMISTRY, 1978, 86 (01) : 159 - 165
  • [9] One-step method for isolation and purification of native β-lactoglobulin from bovine whey
    Stojadinovic, Marija
    Burazer, Lidija
    Ercili-Cura, Dilek
    Sancho, Ana
    Buchert, Johanna
    Velickovic, Tanja Cirkovic
    Stanic-Vucinic, Dragana
    JOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE, 2012, 92 (07) : 1432 - 1440
  • [10] Design of affinity tags for one-step protein purification from immobilized zinc columns
    Pasquinelli, RS
    Shepherd, RE
    Koepsel, RR
    Zhao, A
    Ataai, MM
    BIOTECHNOLOGY PROGRESS, 2000, 16 (01) : 86 - 91