Design of a Genetically Programmable and Customizable Protein Scaffolding System for the Hierarchical Assembly of Robust, Functional Macroscale Materials
Inspired by the properties of natural protein-based biomaterials, protein nanomaterials are increasingly designed with natural or engineered peptides or with protein building blocks. Few examples describe the design of functional protein-based materials for biotechnological applications that can be readily manufactured, are amenable to functionalization, and exhibit robust assembly properties for macroscale material formation. Here, we designed a protein-scaffolding system that self-assembles into robust, macroscale materials suitable for in vitro cell-free applications. By controlling the coexpression in <i>Escherichia coli</i> of self-assembling scaffold building blocks with and without modifications for covalent attachment of cross-linking cargo proteins, hybrid scaffolds with spatially organized conjugation sites are overproduced that can be readily isolated. Cargo proteins, including enzymes, are rapidly cross-linked onto scaffolds for the formation of functional materials. We show that these materials can be used for the in vitro operation of a coimmobilized two-enzyme reaction and that the protein material can be recovered and reused. We believe that this work will provide a versatile platform for the design and scalable production of functional materials with customizable properties and the robustness required for biotechnological applications.
Authors
- Eliana L. Peña (ORCID: https://orcid.org/0000-0002-3055-7382)
- Claudia Schmidt‐Dannert (ORCID: https://orcid.org/0000-0002-0559-3656)
- R. Zhang (ORCID: https://orcid.org/0000-0001-7892-3516)
- François Gaascht (ORCID: https://orcid.org/0000-0001-6129-0708)
- Sun-Young Kang
Institutions
- University of Minnesota (US)
- Biotechnology Institute (US)
Publication Details
- Journal
- ACS Synthetic Biology
- Published
- 2024-10-31
- DOI
- https://doi.org/10.1021/acssynbio.4c00587
- Citations
- 5
- Primary Topic
- 3D Printing in Biomedical Research
- Type
- article
- Field-Weighted Citation Impact
- 0.92
Funders
- Advanced Research Projects Agency - Energy
- Division of Chemical, Bioengineering, Environmental, and Transport Systems