Biotechnology applications of amino acids in protein purification and formulations

被引:175
作者
Arakawa, T.
Tsumoto, K.
Kita, Y.
Chang, B.
Ejima, D.
机构
[1] Alliance Prot Labs, Thousand Oaks, CA 91360 USA
[2] Univ Tokyo, Grad Sch Frontier Sci, Dept Med Genome Sci, Chiba, Japan
[3] Keio Univ, Sch Med, Dept Pharmacol, Tokyo 160, Japan
[4] Integr Biosolut, Camarillo, CA USA
[5] Ajinomoto Co Inc, Amino Sci Labs, Kanagawa, Japan
关键词
protein purification; osmolyte; formulation; lyophilization; aggregation suppression;
D O I
10.1007/s00726-007-0506-3
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
Amino acids are widely used in biotechnology applications. Since amino acids are natural compounds, they can be safely used in pharmaceutical applications, e.g., as a solvent additive for protein purification and as an excipient for protein formulations. At high concentrations, certain amino acids are found to raise intra-cellular osmotic pressure and adjust to the high salt concentrations of the surrounding medium. They are called "compatible solutes", since they do not affect macromolecular function. Not only are they needed to increase the osmotic pressure, they are known to increase the stability of the proteins. Sucrose, glycerol and certain amino acids were used to enhance the stability of unstable proteins after isolation from natural environments. The mechanism of the action of these protein-stabilizing amino acids is relatively well understood. On the contrary, arginine was accidentally discovered as a useful reagent for assisting in the refolding of recombinant proteins. This effect of arginine was ascribed to its ability to suppress aggregation of the proteins during refolding, thereby increasing refolding efficiency. By the same mechanism, arginine now finds much wider applications than previously anticipated in the research and development of proteins, in particular in pharmaceutical applications. For example, arginine solubilizes proteins from loose inclusion bodies, resulting in efficient production of active proteins. Arginine suppresses protein-protein interactions in solution and also non-specific adsorption to gel permeation chromatography columns. Arginine facilitates elution of bound proteins from various column resins, including Protein-A or dye affinity columns and hydrophobic interaction columns. This review covers various biotechnology applications of amino acids, in particular arginine.
引用
收藏
页码:587 / 605
页数:19
相关论文
共 169 条
  • [1] Investigation of refolding condition for Pseudomonas fluorescens lipase by response surface methodology
    Ahn, JH
    Lee, YP
    Rhee, JS
    [J]. JOURNAL OF BIOTECHNOLOGY, 1997, 54 (03) : 151 - 160
  • [2] GLYCINE CRYSTALLIZATION DURING FREEZING - THE EFFECTS OF SALT FORM, PH, AND IONIC-STRENGTH
    AKERS, MJ
    MILTON, N
    BYRN, SR
    NAIL, SL
    [J]. PHARMACEUTICAL RESEARCH, 1995, 12 (10) : 1457 - 1461
  • [3] The effect of formulation excipients on protein stability and aerosol performance of spray-dried powders of a recombinant humanized anti-IgE monoclonal antibody
    Andya, JD
    Maa, YF
    Costantino, HR
    Nguyen, PA
    Dasovich, N
    Sweeney, TD
    Hsu, CC
    Shire, SJ
    [J]. PHARMACEUTICAL RESEARCH, 1999, 16 (03) : 350 - 358
  • [4] PREFERENTIAL INTERACTIONS OF PROTEINS WITH SOLVENT COMPONENTS IN AQUEOUS AMINO-ACID SOLUTIONS
    ARAKAWA, T
    TIMASHEFF, SN
    [J]. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1983, 224 (01) : 169 - 177
  • [5] The effects of protein stabilizers on aggregation induced by multiple-stresses
    Arakawa, T
    Dix, DB
    Chang, BS
    [J]. YAKUGAKU ZASSHI-JOURNAL OF THE PHARMACEUTICAL SOCIETY OF JAPAN, 2003, 123 (11): : 957 - 961
  • [6] The effects of arginine on refolding of aggregated proteins: not facilitate refolding, but suppress aggregation
    Arakawa, T
    Tsumoto, K
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 304 (01) : 148 - 152
  • [7] ARAKAWA T, 1984, J BIOL CHEM, V259, P4979
  • [8] STABILIZATION OF PROTEIN-STRUCTURE BY SUGARS
    ARAKAWA, T
    TIMASHEFF, SN
    [J]. BIOCHEMISTRY, 1982, 21 (25) : 6536 - 6544
  • [9] THE STABILIZATION OF PROTEINS BY OSMOLYTES
    ARAKAWA, T
    TIMASHEFF, SN
    [J]. BIOPHYSICAL JOURNAL, 1985, 47 (03) : 411 - 414
  • [10] THE BASIS FOR TOXICITY OF CERTAIN CRYOPROTECTANTS - A HYPOTHESIS
    ARAKAWA, T
    CARPENTER, JF
    KITA, YA
    CROWE, JH
    [J]. CRYOBIOLOGY, 1990, 27 (04) : 401 - 415