A novel method for the large-scale production of PG-CNP37, a C-type natriuretic peptide analogue

J Biotechnol. 2012 Dec 15;164(2):196-201. doi: 10.1016/j.jbiotec.2012.08.001. Epub 2012 Aug 28.

Abstract

Achondroplasia is the most common form of human dwarfism caused by a mutation in the fibroblast growth factor receptor 3 (FGFR3), resulting in abnormal endochondral bone formation. C-type natriuretic peptide (CNP) is a potent stimulator of endochondral bone growth and represents a potential therapy for achondroplasia. We have developed a novel, simple and cost effective method to produce a CNP analogue, PG-CNP37, at a large scale from Escherichia coli. A PG-CNP37 fusion protein was over-expressed as inclusion bodies in E. coli, which were purified then cleaved by formic acid to release the PG-CNP37 peptide. Approximately 0.5g of 95% pure, soluble and active PG-CNP37 peptide was produced from 1L of culture using this method and may represent a viable means for large-scale production of other therapeutic peptides.

MeSH terms

  • Chromatography, Ion Exchange
  • Cloning, Molecular
  • Escherichia coli / metabolism
  • Formates
  • Inclusion Bodies / metabolism
  • Natriuretic Peptide, C-Type / analogs & derivatives*
  • Natriuretic Peptide, C-Type / chemistry
  • Natriuretic Peptide, C-Type / isolation & purification
  • Natriuretic Peptide, C-Type / metabolism*
  • Recombinant Fusion Proteins / chemistry
  • Recombinant Fusion Proteins / isolation & purification
  • Recombinant Fusion Proteins / metabolism*

Substances

  • Formates
  • Recombinant Fusion Proteins
  • formic acid
  • Natriuretic Peptide, C-Type