Designed modular protein hydrogels for biofabrication
Dalia Dranseike ᵃ, Yusuke Ota ᵇ, Thomas G. W. Edwardson ᵇ, Elia A. Guzzi ᵃ, Mao Hori ᵇ, Zrinka Raguz Nakic ᶜ, Dhananjay V. Deshmukh ᵃ, Mikail D. Levasseur ᵇ, Kevin Mattli ᶜ, Christina M. Tringides ᵈ, Jiangtao Zhou ᵉ, Donald Hilvert ᵇ, Christin Peters ᶜ, Mark W. Tibbitt ᵃ.
- ᵃ Macromolecular Engineering Laboratory, ETH Zurich, Zurich, Switzerland
- ᵇ Organic Chemistry Laboratory, ETH Zurich, Zurich, Switzerland
- ᶜ Biosystems Technology, ZHAW, Wädenswil, Switzerland
- ᵈ Laboratory of Biosensors and Bioelectronics, ETH Zurich, Switzerland
- ᵉ Laboratory of Food and Soft Materials, ETH Zurich, Switzerland
Abstract
Designing proteins that fold and assemble over different length scales provides a way to tailor the mechanical properties and biological performance of hydrogels. In this study, we designed modular proteins that self-assemble into fibrillar networks and, as a result, form hydrogel materials with novel properties. We incorporated distinct functionalities by connecting separate self-assembling (A block) and cell-binding (B block) domains into single macromolecules. The number of self-assembling domains affects the rigidity of the fibers and the final storage modulus G′ of the materials. The mechanical properties of the hydrogels could be tuned over a broad range (G′ = 0.1 – 10 kPa), making them suitable for the cultivation and differentiation of multiple cell types, including cortical neurons and human mesenchymal stem cells. Moreover, we confirmed the bioavailability of cell attachment domains in the hydrogels that can be further tailored for specific cell types or other biological applications. Finally, we demonstrate the versatility of the designed proteins for application in biofabrication as 3D scaffolds that support cell growth and guide their function.
Statement of significance
Designed proteins that enable the decoupling of biophysical and biochemical properties within the final material could enable modular biomaterial engineering. In this context, we present a designed modular protein platform that integrates self-assembling domains (A blocks) and cell-binding domains (B blocks) within a single biopolymer. The linking of assembly domains and cell-binding domains this way provided independent tuning of mechanical properties and inclusion of biofunctional domains. We demonstrate the use of this platform for biofabrication, including neural cell culture and 3D printing of scaffolds for mesenchymal stem cell culture and differentiation. Overall, this work highlights how informed design of biopolymer sequences can enable the modular design of protein-based hydrogels with independently tunable biophysical and biochemical properties.