Liquid–liquid phase separation enables chromatography-free purification and high-performance spidroin-amyloid hybrid silk fibers

K Karin Tufvesson (Department of Animal Biosciences, Swedish University of Agricultural Sciences) V Viktoria Langwallner (Department of Animal Biosciences, Swedish University of Agricultural Sciences) T Tomas Bohn Pessatti (Department of Animal Biosciences, Swedish University of Agricultural Sciences) G Gabriele Greco (Department of Animal Biosciences, Swedish University of Agricultural Sciences) E Elin Karlsson (Department of Animal Biosciences, Swedish University of Agricultural Sciences) S Sarah Stadlmayr (Department of Medicine Huddinge, Karolinska Institutet) A Axel Leppert M Michael Landreh (Department of Cell and Molecular Biology, Uppsala University, Uppsala, Sweden.) A Anna Rising (Department of Animal Biosciences, Swedish University of Agricultural Sciences) B Benjamin Schmuck (Department of Animal Biosciences, Swedish University of Agricultural Sciences)

Abstract

Large-scale production of artificial spider silk fibers requires heterologous expression of spider silk proteins (spidroins), yet current methods remain limited by low yields and costly purification processes. To overcome these challenges, we engineered mini-spidroins in which the poly-alanine motifs of the repetitive region were replaced with the non-natural amyloidogenic β16 peptide, significantly enhancing expression yields and solubility. Furthermore, we developed a simple, chromatography-free purification method for these constructs based on NaCl-induced liquid–liquid phase separation (LLPS). This one-step purification strategy reduced processing costs by up to 99% compared to conventional affinity chromatography while achieving yields of ~300 mg of purified protein per liter of shake flask culture and ~25 g L −1 from bioreactor cultivations. The purified engineered mini-spidroins could be spun into continuous fibers using an all-aqueous, biomimetic spinning process triggered by a pH drop. The resulting fibers exhibited mechanical properties comparable to those produced from the mini-spidroin NT2RepCT, which requires conventional chromatographic purification. Together, our protein-engineering approach and LLPS-based purification method provide a potentially scalable, sustainable, and cost-effective platform for artificial spider silk, representing a major step toward the commercial viability of recombinant silk-based materials.

Article Details

Volume / Issue Vol. 123, Issue 28
Published July 14, 2026
ISSN 0027-8424
Publisher National Academy of Sciences

Authors (10)

K

Karin Tufvesson

Department of Animal Biosciences, Swedish University of Agricultural Sciences

V

Viktoria Langwallner

Department of Animal Biosciences, Swedish University of Agricultural Sciences

T

Tomas Bohn Pessatti

Department of Animal Biosciences, Swedish University of Agricultural Sciences

G

Gabriele Greco

Department of Animal Biosciences, Swedish University of Agricultural Sciences

E

Elin Karlsson

Department of Animal Biosciences, Swedish University of Agricultural Sciences

S

Sarah Stadlmayr

Department of Medicine Huddinge, Karolinska Institutet

A

Axel Leppert

M

Michael Landreh

Department of Cell and Molecular Biology, Uppsala University, Uppsala, Sweden.

A

Anna Rising

Department of Animal Biosciences, Swedish University of Agricultural Sciences

B

Benjamin Schmuck

Department of Animal Biosciences, Swedish University of Agricultural Sciences