Literature DB >> 16325191

Comparison of protein A affinity sorbents III. Life time study.

Rainer Hahn1, Kazumichi Shimahara, Franz Steindl, Alois Jungbauer.   

Abstract

Protein A affinity chromatography is a popular purification method for immunoglobulins applied at various scales, ranging from micro-tube up to 1000l 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.

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Year:  2005        PMID: 16325191     DOI: 10.1016/j.chroma.2005.10.083

Source DB:  PubMed          Journal:  J Chromatogr A        ISSN: 0021-9673            Impact factor:   4.759


  8 in total

1.  Remarkable alkaline stability of an engineered protein A as immunoglobulin affinity ligand: C domain having only one amino acid substitution.

Authors:  Kazunobu Minakuchi; Dai Murata; Yuji Okubo; Yoshiyuki Nakano; Shinichi Yoshida
Journal:  Protein Sci       Date:  2013-08-06       Impact factor: 6.725

2.  Antibody purification via affinity membrane chromatography method utilizing nucleotide binding site targeting with a small molecule.

Authors:  Nur Mustafaoglu; Tanyel Kiziltepe; Basar Bilgicer
Journal:  Analyst       Date:  2016-11-28       Impact factor: 4.616

3.  Evaluation of a novel methacrylate-based Protein A resin for the purification of immunoglobulins and Fc-fusion proteins.

Authors:  Tyler R McCaw; Edward K Koepf; Lynn Conley
Journal:  Biotechnol Prog       Date:  2014-07-24

4.  In-column ATR-FTIR spectroscopy to monitor affinity chromatography purification of monoclonal antibodies.

Authors:  Maxime Boulet-Audet; Sergei G Kazarian; Bernadette Byrne
Journal:  Sci Rep       Date:  2016-07-29       Impact factor: 4.379

5.  Linear flow-velocity gradient chromatography-An efficient method for increasing the process efficiency of batch and continuous capture chromatography of proteins.

Authors:  Chyi-Shin Chen; Kosei Ando; Noriko Yoshimoto; Shuichi Yamamoto
Journal:  Biotechnol Bioeng       Date:  2021-01-03       Impact factor: 4.530

6.  Cleaning-in-place of immunoaffinity resins monitored by in situ ATR-FTIR spectroscopy.

Authors:  Maxime Boulet-Audet; Bernadette Byrne; Sergei G Kazarian
Journal:  Anal Bioanal Chem       Date:  2015-07-10       Impact factor: 4.142

7.  Real-time monitoring and control of the load phase of a protein A capture step.

Authors:  Matthias Rüdt; Nina Brestrich; Laura Rolinger; Jürgen Hubbuch
Journal:  Biotechnol Bioeng       Date:  2016-09-21       Impact factor: 4.530

8.  The pearl necklace model in protein A chromatography: Molecular mechanisms at the resin interface.

Authors:  Goncalo L Silva; Jacek Plewka; Helga Lichtenegger; Ana C Dias-Cabral; Alois Jungbauer; Rupert Tscheließnig
Journal:  Biotechnol Bioeng       Date:  2018-10-25       Impact factor: 4.530

  8 in total

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