Coating with genetic engineered hydrophobin promotes growth of fibroblasts on a hydrophobic solid

Biomaterials. 2002 Dec;23(24):4847-54. doi: 10.1016/s0142-9612(02)00240-5.

Abstract

Class I Hydrophobins self-assemble at hydrophilic-hydrophobic interfaces into a highly insoluble amphipathic film. Upon self-assembly of these fungal proteins hydrophobic solids turn hydrophilic, while hydrophilic materials can be made hydrophobic. Hydrophobins thus change the nature of a surface. This property makes them interesting candidates to improve physio- and physico-chemical properties of implant surfaces. We here show that growth of fibroblasts on Teflon can be improved by coating the solid with genetically engineered SC3 hydrophobin. Either deleting a stretch of 25 amino acids at the N-terminus of the mature hydrophobin (TrSC3) or fusing the RGD peptide to this end (RGD-SC3) improved growth of fibroblasts on the solid surface. In addition, we have shown that assembled SC3 and TrSC3 are not toxic when added to the medium of a cell culture of fibroblasts in amounts up to 125 microg ml(-1).

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Cell Division
  • Cell Line
  • Cells, Cultured
  • Coated Materials, Biocompatible / pharmacology*
  • Coloring Agents / pharmacology
  • Fibroblasts / metabolism*
  • Fungal Proteins / genetics
  • Fungal Proteins / pharmacology*
  • Gene Deletion
  • Genetic Engineering*
  • Mice
  • Molecular Sequence Data
  • Peptides / chemistry
  • Polytetrafluoroethylene / pharmacology
  • Protein Structure, Tertiary
  • Schizophyllum / metabolism
  • Sequence Homology, Amino Acid
  • Tetrazolium Salts / pharmacology
  • Thiazoles / pharmacology
  • Time Factors

Substances

  • Coated Materials, Biocompatible
  • Coloring Agents
  • Fungal Proteins
  • Peptides
  • Tetrazolium Salts
  • Thiazoles
  • Polytetrafluoroethylene
  • thiazolyl blue