Zaki, M. orcid.org/0009-0003-8050-5390, Greco, G., Moreno-Tortolero, R.O. et al. (2 more authors) (2026) A perspective on the evolution of artificial silk fibre research. Communications Materials, 7 (1). 159. ISSN: 2662-4443
Abstract
For over a century, artificial silk spinning has pursued the exceptional mechanical performance of natural fibres, largely through a molecular-centric strategy. Limitations in artificial systems have been attributed to insufficient molecular weight, incomplete sequence architecture, or loss of native terminal domains, factors also thought to disrupt liquid-liquid phase separation (LLPS) and hierarchical assembly. LLPS is proposed to concentrate and pre-organise silk proteins, facilitating alignment during spinning and formation of hierarchical structures that underpin mechanical performance. Here, we reevaluate this paradigm through comparisons of regenerated silk fibroin (RSF), recombinant silk proteins, and regenerated undegummed silk (RUS). Advances across these systems have substantially narrowed the molecular gap with native silk, and under optimised conditions, all can produce fibres with comparable mechanical properties. While LLPS and hierarchical organisation can be induced in RSF and recombinant systems, these features do not consistently improve mechanics, suggesting native-like assembly alone is insufficient. RUS, which retains multicomponent interactions, most closely reflects the native system, yet still exhibits distinct rheology. Collectively, this indicates that artificial dopes lack compositional complexity and ability to respond to dynamic physiochemical gradients of the silk gland. Future progress in artificial spinning will require reconstructing the multicomponent, non-equilibrium environment governing silk assembly in nature.
Metadata
| Item Type: | Article |
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| Authors/Creators: |
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| Copyright, Publisher and Additional Information: | © The Author(s) 2026. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
| Keywords: | Biomaterials – proteins |
| Dates: |
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| Institution: | The University of Sheffield |
| Academic Units: | The University of Sheffield > Faculty of Engineering (Sheffield) > School of Chemical, Materials and Biological Engineering |
| Date Deposited: | 30 Jun 2026 07:43 |
| Last Modified: | 30 Jun 2026 07:43 |
| Status: | Published |
| Publisher: | Springer Science and Business Media LLC |
| Refereed: | Yes |
| Identification Number: | 10.1038/s43246-026-01232-8 |
| Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:242676 |
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