A general vector, pASK84, for cloning, bacterial production, and single-step purification of antibody Fab fragments

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Abstract

The expression vector pASK84 was designed for the convenient cloning of immunoglobulin variable domain genes, as well as periplasmic secretion of the corresponding Fab fragment in Escherichia coli. The plasmid provides the constant domain genes of mouse IgG1/K with a hexa-histidine tag fused to the C terminus of the heavy chain. This strategy enables the rapid and efficient purification of the functional recombinant Fab fragment via immobilized metal affinity chromatography. The versatility of this expression and purification system is demonstrated using the variable domains of the well-characterized anti-lysozyme antibody D1.3.

Original languageEnglish
Pages (from-to)79-84
Number of pages6
JournalGene
Volume141
Issue number1
DOIs
StatePublished - 8 Apr 1994
Externally publishedYes

Keywords

  • Escherichia coli
  • iminodiacetic acid-Sepharose
  • immobilized metal affinity chromatography
  • immunoglobulin
  • oligo-histidine tag
  • secretion

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