Literature DB >> 12790654

Efficient inclusion body processing using chemical extraction and high gradient magnetic fishing.

Anders Heebøll-Nielsen1, Woo-Seok Choe, Anton P J Middelberg, Owen R T Thomas.   

Abstract

In this study we introduce a radical new approach for the recovery of proteins expressed in the form of inclusion bodies, involving (i) chemical extraction from the host cells, (ii) adsorptive capture of the target protein onto small magnetic adsorbents, and (iii) subsequent rapid collection of the product-loaded supports with the aid of high gradient magnetic fields. The manufacture and testing of two types of micron-sized nonporous superparamagnetic metal chelator particles derivatized with iminodiacetic acid is described. In small-scale adsorption studies conducted with a hexahistidine tagged form of the L1 coat protein of human papillomavirus type 16 dissolved in 8 M urea-phosphate buffer, the best binding performance (Q(max) = 58 mg g(-1) and K(d) approximately 0.08 microM) was exhibited by Cu(2+)-charged type II support materials. Equilibrium adsorption of L1 to these nonporous supports was achieved very rapidly (<300 s), and approximately 90% of the tightly bound L1 could be desorbed in just one elution step by including >100 mM imidazole in the equilibration buffer. The influence of feedstock complexity on L1 adsorption to the Cu(2+)-charged type II magnetic chelators was studied using various dilutions of four crude chemical E. coli cell extracts containing denatured L1 protein. Undiminished L1 adsorption to these adsorbents (relative to the 8 M urea-phosphate buffer case) was observed with the least complex of these feed materials, i.e., a partially clarified (12 g dry weight L(-1)) and spermine-treated chemical cell extract (feedstock B). Efficient recovery of L1 from feed B was demonstrated at a 60-fold increased scale using the high gradient magnetic fishing (HGMF) system to collect loaded Cu(2+)-chelator particles following batch adsorption of L1. Over 70% of the initial L1 present was recovered within the HGMF rig in a highly clarified form in two batch elution cycles with an overall purification factor of approximately 10.

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Year:  2003        PMID: 12790654     DOI: 10.1021/bp025553n

Source DB:  PubMed          Journal:  Biotechnol Prog        ISSN: 1520-6033


  4 in total

1.  A novel system for continuous protein refolding and on-line capture by expanded bed adsorption.

Authors:  Henrik Ferré; Emmanuel Ruffet; Lise-Lotte B Nielsen; Mogens Holst Nissen; Timothy J Hobley; Owen R T Thomas; Søren Buus
Journal:  Protein Sci       Date:  2005-08       Impact factor: 6.725

2.  Magnetic techniques for the isolation and purification of proteins and peptides.

Authors:  Ivo Safarik; Mirka Safarikova
Journal:  Biomagn Res Technol       Date:  2004-11-26

3.  Strategies for the recovery of active proteins through refolding of bacterial inclusion body proteins.

Authors:  Luis Felipe Vallejo; Ursula Rinas
Journal:  Microb Cell Fact       Date:  2004-09-02       Impact factor: 5.328

4.  Magnetic hydrophobic-charge induction adsorbents for the recovery of immunoglobulins from antiserum feedstocks by high-gradient magnetic fishing.

Authors:  Cláudia Sg Gomes; Adedayo Fashina; Alfred Fernández-Castané; Timothy W Overton; Timothy J Hobley; Eirini Theodosiou; Owen Rt Thomas
Journal:  J Chem Technol Biotechnol       Date:  2018-03-30       Impact factor: 3.174

  4 in total

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