• Title of article

    Comparison of protein A affinity sorbents III. Life time study

  • Author/Authors

    Hahn، نويسنده , , Rainer and Shimahara، نويسنده , , Kazumichi and Steindl، نويسنده , , Franz and Jungbauer، نويسنده , , Alois، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2006
  • Pages
    8
  • From page
    224
  • To page
    231
  • Abstract
    Protein A affinity chromatography is a popular purification method for immunoglobulins applied at various scales, ranging from micro-tube up to 1000 l column format. Three novel high capacity protein A affinity chromatography media have been subjected to a lifetime study using 50 consecutive purification cycles of a cell culture supernatant (CCS) containing a monoclonal antibody. Chromatographic conditions followed protocols used in industrial antibody processing, including stripping and cleaning-in-place of the resins. For all three media, no significant loss of purification performance (measured by sodium dodecylsulfate polyacrylamide gel electrophoresis and analytical size-exclusion chromatography (SEC)) could be observed over 50 cycles. Eluate samples were analyzed for leaked protein A and host cell protein (HCP) content. MabSelect SuRe, the first protein A affinity medium compatible with alkaline regeneration conditions, exhibited the lowest leakage levels, in the range of 1–3 ppm. For the media MabSelect Xtra and ProSep-vA Ultra, leakage levels were in the range of 30–40 ppm. Host cell protein content of eluates from MabSelect Xtra and SuRe were between 300 and 700 ppm, whereas for ProSep-vA Ultra 3000–4000 ppm was achieved.
  • Keywords
    Leakage , Immunoglobulin , Antibody , Staphylococcus protein A , Host cell protein
  • Journal title
    Journal of Chromatography A
  • Serial Year
    2006
  • Journal title
    Journal of Chromatography A
  • Record number

    1524985