Affitins for protein purification by affinity magnetic fishing

Cláudia S M Fernandes, Raquel Marta Neves dos Santos Garcia, Stella Ottengy, Aline Canani Viecinski, Ghislaine Béhar, Barbara Mouratou, Frédéric Pecorari, A Cecília A Roque

Research output: Contribution to journalArticlepeer-review

17 Citations (Scopus)

Abstract

Currently most economical and technological bottlenecks in protein production are placed in the downstream processes. With the aim of increasing the efficiency and reducing the associated costs, various affinity ligands have been developed. Affitins are small, yet robust and easy to produce, proteins derived from the archaeal extremophilic "7kDa DNA-binding" protein family. By means of combinatorial protein engineering and ribosome display selection techniques, Affitins have shown to bind a diversity of targets. In this work, two previously developed Affitins (anti-lysozyme and anti-IgG) were immobilized onto magnetic particles to assess their potential for protein purification by magnetic fishing. The optimal lysozyme and human IgG binding conditions yielded 58mg lysozyme/g support and 165mgIgG/g support, respectively. The recovery of proteins was possible in high yield (≥95%) and with high purity, namely ≥95% and 81%, when recovering lysozyme from Escherichia coli supernatant and IgG from human plasma, respectively. Static binding studies indicated affinity constants of 5.0×10(4)M(-1) and 9.3×10(5)M(-1) for the anti-lysozyme and anti-IgG magnetic supports. This work demonstrated that Affitins, which can be virtually evolved for any protein of interest, can be coupled onto magnetic particles creating novel affinity adsorbents for purification by magnetic fishing.

Original languageEnglish
Pages (from-to)50-58
Number of pages9
JournalJournal Of Chromatography A
Volume1457
DOIs
Publication statusPublished - 29 Jul 2016

Keywords

  • BINDING-PROTEINS
  • MONOCLONAL-ANTIBODIES
  • PHAGE DISPLAY
  • SECRETIN PULD
  • EGG-WHITE
  • NANOPARTICLES
  • LYSOZYME
  • DNA
  • SEPARATIONS
  • SUPERNATANT

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