Silk-Silk Interactions between Silkworm Fibroin and Recombinant Spider Silk Fusion Proteins Enable the Construction of Bioactive Materials

ACS Appl Mater Interfaces. 2017 Sep 20;9(37):31634-31644. doi: 10.1021/acsami.7b10874. Epub 2017 Sep 11.

Abstract

Natural silk is easily accessible from silkworms and can be processed into different formats suitable as biomaterials and cell culture matrixes. Recombinant DNA technology enables chemical-free functionalization of partial silk proteins through fusion with peptide motifs and protein domains, but this constitutes a less cost-effective production process. Herein, we show that natural silk fibroin (SF) can be used as a bulk material that can be top-coated with a thin layer of the recombinant spider silk protein 4RepCT in fusion with various bioactive motifs and domains. The coating process is based on a silk assembly to achieve stable interactions between the silk types under mild buffer conditions. The assembly process was studied in real time by quartz crystal microbalance with dissipation. Coatings, electrospun mats, and microporous scaffolds were constructed from Antheraea assama and Bombyx mori SFs. The morphology of the fibroin materials before and after coating with recombinant silk proteins was analyzed by scanning electron microscopy and atomic force microscopy. SF materials coated with various bioactive 4RepCT fusion proteins resulted in directed antibody capture, enzymatic activity, and improved cell attachment and spreading, respectively, compared to pristine SF materials. The herein-described procedure allows a fast and easy route for the construction of bioactive materials.

Keywords: biomaterial; functionalization; recombinant spider silk; self-assembly; silk fibroin.

MeSH terms

  • Animals
  • Biocompatible Materials
  • Bombyx
  • Fibroins / chemistry*
  • Recombinant Fusion Proteins
  • Silk

Substances

  • Biocompatible Materials
  • Recombinant Fusion Proteins
  • Silk
  • Fibroins