Functionalized silk assembled from a recombinant spider silk fusion protein (Z-4RepCT) produced in the methylotrophic yeast Pichia pastoris
2016 (English)In: Biotechnology Journal, ISSN 1860-6768, E-ISSN 1860-7314, Vol. 11, no 5, 687-699 p.Article in journal (Refereed) PublishedText
Functional biological materials are a growing research area with potential applicability in medicine and biotechnology. Using genetic engineering, the possibility to introduce additional functions into spider silk-based materials has been realized. Recently, a recombinant spider silk fusion protein, Z-4RepCT, was produced intracellularly in Escherichia coli and could after purification self-assemble into silk-like fibers with ability to bind antibodies via the IgG-binding Z domain. In this study, the use of the methylotrophic yeast Pichia pastoris for production of Z-4RepCT has been investigated. Temperature, pH and production time were influencing the amount of soluble Z-4RepCT retrieved from the extracellular fraction. Purification of secreted Z-4RepCT resulted in a mixture of full-length and degraded silk proteins that failed to self-assemble into fibers. A position in the C-terminal domain of 4RepCT was identified as being subjected to proteolytic cleavage by proteases in the Pichia culture supernatant. Moreover, the C-terminal domain was subjected to glycosylation during production in P. pastoris. These observed alterations of the CT domain are suggested to contribute to the failure in fiber assembly. As alternative approach, Z-4RepCT retrieved from the intracellular fraction, which was less degraded, was used and shown to retain ability to assemble into silk-like fibers after enzymatic deglycosylation.
Place, publisher, year, edition, pages
Wiley-VCH Verlagsgesellschaft, 2016. Vol. 11, no 5, 687-699 p.
Glycosylation, Heterologous protein expression, Intracellular/extracellular protein, Pichia pastoris, Recombinant spider silk, Bins, Biological materials, Enzyme activity, Escherichia coli, Fibers, Genetic engineering, Purification, Recombinant proteins, Yeast, C-terminal domains, Culture supernatant, Deglycosylation, Heterologous proteins, Methylotrophic yeasts, Proteolytic cleavage, Spider silks, Proteins
IdentifiersURN: urn:nbn:se:kth:diva-186986DOI: 10.1002/biot.201500412ISI: 000375078600011ScopusID: 2-s2.0-84960156082OAI: oai:DiVA.org:kth-186986DiVA: diva2:929404
FunderKnut and Alice Wallenberg Foundation, 2013-883Swedish Research Council, VR-NT 2013-6104VINNOVASwedish Research Council Formas, 2013-883
QC 201605182016-05-182016-05-162016-05-30Bibliographically approved