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Sterilized Recombinant Spider Silk Fibers of Low Pyrogenicity

  • My Hedhammar
  • , Hanna Bramfeldt
  • , Teodora Baris
  • , Mona Widhe
  • , Glareh Askarieh
  • , Kerstin Nordling
  • , Sonja von Aulock
  • , Jan Johansson

    Publication: Contribution to journalJournal articlepeer-review

    Abstract

    We have recently shown that it is possible to recombinantly produce a miniature spider silk protein, 4RepCT, that spontaneously self-assembles into mechanically stable macroscopic fibers (Stark, M.; Grip, S.; Rising, A.; Hedhammar, M.; Engstrom, W.; Hjalm, G.; Johansson, J. Macroscopic fibers self-assembled from recombinant miniature spider silk proteins. Biomacromolecules 2007, 8 (5), 1695-1701). When produced as a soluble fusion protein (with thioredoxin) in Escherichia con, the spider silk protein can be subjected to several purification steps without aggregating. Here, combined purification and endotoxin removal is achieved using a simple cell wash procedure, protein affinity purification, and LIDS depletion. No toxic chemicals were included in the process and the protein retained its ability to self-assemble into fibers. With this method, fibers with pyrogenicity corresponding to less than 1 EU/mg could be recovered. Moreover, the fibers could be sterilized through autoclaving with retained morphology, structure, and mechanical properties. This implies that this recombinant silk is suitable for usage as biomaterial, which is further supported by data showing that the fibers allow growth of human primary fibroblasts.
    Original languageEnglish
    Pages (from-to)953-959
    Number of pages7
    JournalBiomacromolecules
    Volume11
    Issue number4
    DOIs
    Publication statusPublished - 2010

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