Single pH buffer refolding screen for protein from inclusion bodies

Protein Expr Purif. 2012 Apr;82(2):352-9. doi: 10.1016/j.pep.2012.01.014. Epub 2012 Feb 4.

Abstract

We previously reported the set up of an automated test for screening the refolding of recombinant proteins expressed as inclusion bodies in Escherichia coli[1]. The screen used 96 refolding buffers and was validated with 24 proteins, 70% of which remained soluble in at least one buffer. In the present paper, we have analyzed in more detail these experimental data to see if the refolding process can be driven by general rules. Notably, we found that proteins with an acidic isoelectric point (pI) refolded in buffers the average pH of which was alkaline and conversely. In addition, the number of refolding buffers wherein a protein remained soluble increased with the difference between its pI and the average pH of the buffers in which it refolded. A trend analysis of the other variables (ionic strength, detergents, etc.) was also performed. On the basis of this analysis, we devised and validated a new refolding screen made of a single buffer for acidic proteins and a single buffer for alkaline proteins.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins / chemistry
  • Bacterial Proteins / isolation & purification
  • Base Sequence
  • Carboxylic Ester Hydrolases / chemistry
  • Carboxylic Ester Hydrolases / isolation & purification
  • DNA Primers / genetics
  • Escherichia coli
  • Humans
  • Hydrogen-Ion Concentration
  • Inclusion Bodies / chemistry*
  • Indicators and Reagents
  • Isoelectric Point
  • Molecular Sequence Data
  • Protein Refolding*
  • Proteome / chemistry
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / isolation & purification
  • Solubility

Substances

  • Bacterial Proteins
  • DNA Primers
  • Indicators and Reagents
  • Proteome
  • Recombinant Proteins
  • Carboxylic Ester Hydrolases
  • Rv1399c protein, M tuberculosis
  • feruloyl esterase