Diepoxide-triggered conformational transition of silk fibroin: formation of hydrogels

Biomacromolecules. 2012 Apr 9;13(4):1122-8. doi: 10.1021/bm300006r. Epub 2012 Mar 6.

Abstract

Silk fibroin hydrogels with tunable properties could be obtained from aqueous fibroin solutions (4.2 w/v %) in a short period of time. This was achieved by the addition of ethylene glycol diglycidyl ether (EGDE) into the reaction solution. Introduction of EGDE cross-links between the fibroin molecules decreases the mobility of the chains, which triggers the conformational transition from random-coil to β-sheet structure and hence fibroin gelation. Dynamic rheological measurements conducted at 50 °C show the formation of strong to weak hydrogels depending on the pH of the reaction solution. Although EGDE attacks the amino groups of fibroin and forms interstrand cross-links, β-sheets acting as physical cross-links dominate the elasticity of the hydrogels. Mechanical response of low-modulus fibroin hydrogels formed above pH 9.7 is highly nonlinear with strong strain hardening behavior (700%) arising from the alignment of the crystallizable amino acid segments.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cross-Linking Reagents / chemical synthesis*
  • Cross-Linking Reagents / chemistry
  • Epoxy Resins / chemistry*
  • Fibroins / chemistry*
  • Gels / chemical synthesis
  • Gels / chemistry
  • Hydrogels / chemical synthesis*
  • Hydrogels / chemistry
  • Hydrogen-Ion Concentration
  • Molecular Conformation
  • Rheology
  • Silk / chemistry*
  • Solutions
  • Water / chemistry

Substances

  • Cross-Linking Reagents
  • Epoxy Resins
  • Gels
  • Hydrogels
  • Silk
  • Solutions
  • Water
  • Quetol 651
  • Fibroins