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MEP chromatography of antibody and Fc-fusion protein using aqueous arginine solution.
Arakawa, Tsutomu; Kita, Yoshiko; Sato, Haruna; Ejima, Daisuke.
Afiliación
  • Arakawa T; Alliance Protein Laboratories, Inc., 3957 Corte Cancion, Thousand Oaks, CA 91360-6919, USA. tarakawa2@aol.com
Protein Expr Purif ; 63(2): 158-63, 2009 Feb.
Article en En | MEDLINE | ID: mdl-18848995
ABSTRACT
MEP HyperCel resin, one of the Protein-A mimetic columns, is designed to bind antibodies at physiological pH and elutes the bound antibodies at mildly acidic pH. We have tested aqueous arginine solution for washing and elution of the resin. To our surprise, bound antibody and Fc-fusion protein eluted at pH 7.0 using 1M arginine solution. Various solvent additives were then examined at pH 7.0. Among the tested additives, urea and arginine were the only additives that were effective in elution. Thus, urea and arginine at low concentrations were effectively used for washing the resin. NaCl and MgCl(2) at 0.1-1M and ethanol at 5-20% were not effective. Based on these observations, it appears that protein binds to MEP resin through both polar and hydrophobic interactions with some contribution of electrostatic interaction, which can be simultaneously reduced by arginine or urea. On the other hand, Mabsorbent, another Protein-A mimetic column, appears to be more non-specific and non-selective.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas Recombinantes de Fusión / Fragmentos Fc de Inmunoglobulinas / Cromatografía de Afinidad / Químicos de Laboratorio / Anticuerpos Idioma: En Revista: Protein Expr Purif Asunto de la revista: BIOLOGIA MOLECULAR Año: 2009 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas Recombinantes de Fusión / Fragmentos Fc de Inmunoglobulinas / Cromatografía de Afinidad / Químicos de Laboratorio / Anticuerpos Idioma: En Revista: Protein Expr Purif Asunto de la revista: BIOLOGIA MOLECULAR Año: 2009 Tipo del documento: Article País de afiliación: Estados Unidos