1. Academic Validation
  2. Total synthesis of desB30 insulin analogues by biomimetic folding of single-chain precursors

Total synthesis of desB30 insulin analogues by biomimetic folding of single-chain precursors

  • Chembiochem. 2008 Dec 15;9(18):2989-96. doi: 10.1002/cbic.200800430.
A Pernille Tofteng 1 Knud J Jensen Lauge Schäffer Thomas Hoeg-Jensen
Affiliations

Affiliation

  • 1 Faculty of Life Sciences, University of Copenhagen, Frederiksberg, Denmark.
Abstract

Insulin is a peptide hormone consisting of 51 Amino acids in two chains with three disulfide bridges. Human Insulin and various analogues are used for the treatment of diabetes and are produced recombinantly at ton scale. Herein, we report the chemical synthesis of Insulin by the step-wise, Fmoc-based, solid-phase synthesis of single-chain precursors with solubilising extensions, which under redox conditions, spontaneously fold with the correct pairing of the three disulfide bridges. The folded, single-chain, Insulin precursors can be transformed into bioactive two-chain desB30 Insulin by the simultaneous removal of the solubilising extension (4-5 residues) and the chain-bridging C-peptide (3-5 residues) by employing Achromobacter lyticus protease--a process well-known from the yeast-based recombinant production of Insulin. The overall yields of synthetic insulins were as much as 6 %, and the synthetic process was straightforward and not labour intensive.

Figures
Products