RETRACTED: Pilot production of recombinant human clotting factor IX from transgenic sow milk (Retracted article. See vol. 926, pg. 108, 2013)

被引:6
作者
Sun, Yu-ling [1 ]
Chang, Yuo-sheng [1 ]
Lin, Yin-shen [1 ]
Yen, Chon-ho [1 ]
机构
[1] Anim Technol Inst Taiwan, Div Biotechnol, Chunan 350, Miaoli, Taiwan
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2012年 / 898卷
关键词
Factor IX; Transgenic sow; Milk; Purification; HUMAN PROTEIN-C; PURITY FACTOR-IX; MANUFACTURING PROCESS; GAMMA-CARBOXYLATION; BLOOD-COAGULATION; MOLECULAR-BASIS; MAMMARY-GLAND; EXPRESSION; PURIFICATION; PIGS;
D O I
10.1016/j.jchromb.2012.04.022
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Valuable pharmaceutical proteins produced from the mammary glands of transgenic livestock have potential use in the biomedical industry. In this study, recombinant human clotting factor IX (rhFIX) produced from transgenic sow milk for preclinical animal studies have been established. The transgenic sow milk was skimmed and treated with sodium phosphate buffer to remove abundant casein protein. Then, the gamma-carboxylated rhFIX fraction was segregated through the Q Sepharose chromatography from uncarboxylated one. For safety issue, the process included virus inactivation by solvent/detergent (S/D) treatment. Subsequently, the S/D treated sample was loaded into the Heparin Sepharose column to recover the rhFIX fraction, which was then reapplied to the Heparin Sepharose column to enhance rhFIX purity and lower the ratio of activated form rhFIX (rhFIXa) easily. This was possible due to the higher affinity of the Heparin affinity sorbent for rhFIXa than for the rhFIX zymogen. Furthermore, an IgA removal column was used to eliminate porcine IgA in purified rhFIX. Finally, nanofiltration was performed for viral clearance. Consequently, a high-quality rhFIX product was produced (approximately 700 mg per batch). Other values for final rhFIX preparation were as follows: purity, >99%; average specific activity, 415.6 +/- 57.7 IU/mL and total milk impurity, <0.5 ng/mg. This is the first report that described the whole process and stable production of bioactive rhFIX from transgenic sow milk. The overall manufacturing process presented here has the potential for industrial production of rhFIX for treatment of hemophilia B patients. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:78 / 89
页数:12
相关论文
共 41 条
  • [1] PURIFICATION AND CHARACTERIZATION OF HUMAN FACTOR 9
    ANDERSSON, LO
    BORG, H
    MILLERANDERSSON, M
    [J]. THROMBOSIS RESEARCH, 1975, 7 (03) : 451 - 459
  • [2] EXPRESSION OF ACTIVE HUMAN CLOTTING FACTOR-IX FROM RECOMBINANT DNA CLONES IN MAMMALIAN-CELLS
    ANSON, DS
    AUSTEN, DEG
    BROWNLEE, GG
    [J]. NATURE, 1985, 315 (6021) : 683 - 685
  • [3] The carboxylation efficiency of the vitamin K-dependent clotting factors: studies with factor IX
    Blostein, M.
    Cuerquis, J.
    Landry, S.
    Galipeau, J.
    [J]. HAEMOPHILIA, 2008, 14 (05) : 1063 - 1068
  • [4] EXPRESSION OF ACTIVE HUMAN FACTOR-IX IN TRANSFECTED CELLS
    BUSBY, S
    KUMAR, A
    JOSEPH, M
    HALFPAP, L
    INSLEY, M
    BERKNER, K
    KURACHI, K
    WOODBURY, R
    [J]. NATURE, 1985, 316 (6025) : 271 - 273
  • [5] Chang CH, 2008, IN VIVO, V22, P693
  • [6] Chang JT, 2010, JPN J VET RES, V58, P179
  • [7] Sustained Release of Transgenic Human Factor IX: Preparation, Characterization, and in Vivo Efficacy
    Chang, Li-Chien
    Yang, Chi-Yu
    Chua, Anna Chian New
    Lin, Yi-Juain
    Lai, Sun-Mou
    [J]. MOLECULAR PHARMACEUTICS, 2011, 8 (05) : 1767 - 1774
  • [8] Recombinant factor IX (BeneFix®) by adjusted continuous infusion:: a study of stability, sterility and clinical experience
    Chowdary, P
    Dasani, H
    Jones, JAH
    Loran, CM
    Eldridge, A
    Hughes, S
    Collins, PW
    [J]. HAEMOPHILIA, 2001, 7 (02) : 140 - 145
  • [9] EXPRESSION OF HUMAN ANTI-HEMOPHILIC FACTOR-IX IN THE MILK OF TRANSGENIC SHEEP
    CLARK, AJ
    BESSOS, H
    BISHOP, JO
    BROWN, P
    HARRIS, S
    LATHE, R
    MCCLENAGHAN, M
    PROWSE, C
    SIMONS, JP
    WHITELAW, CBA
    WILMUT, I
    [J]. BIO-TECHNOLOGY, 1989, 7 (05): : 487 - 492
  • [10] The mammary gland as a bioreactor: Expression, processing, and production of recombinant proteins
    Clark, AJ
    [J]. JOURNAL OF MAMMARY GLAND BIOLOGY AND NEOPLASIA, 1998, 3 (03) : 337 - 350