Affiliation:
1. Department of Materials Science & Engineering Stanford University Stanford CA 94305 USA
2. Department of Biomedical Engineering University of California Davis 451 Health Sciences Dr, GBSF 3315 Davis CA 95616 USA
3. Department of Materials Science & Engineering 476 Lomita Mall, McCullough Room 246 Stanford CA 94305 USA
Abstract
AbstractThe biochemical and biophysical properties of the extracellular matrix (ECM) play a pivotal role in regulating cellular behaviors such as proliferation, migration, and differentiation. Engineered protein‐based hydrogels, with highly tunable multifunctional properties, have the potential to replicate key features of the native ECM. Formed by self‐assembly or crosslinking, engineered protein‐based hydrogels can induce a range of cell behaviors through bioactive and functional domains incorporated into the polymer backbone. Using recombinant techniques, the amino acid sequence of the protein backbone can be designed with precise control over the chain‐length, folded structure, and cell‐interaction sites. In this review, the modular design of engineered protein‐based hydrogels from both a molecular‐ and network‐level perspective are discussed, and summarize recent progress and case studies to highlight the diverse strategies used to construct biomimetic scaffolds. This review focuses on amino acid sequences that form structural blocks, bioactive blocks, and stimuli‐responsive blocks designed into the protein backbone for highly precise and tunable control of scaffold properties. Both physical and chemical methods to stabilize dynamic protein networks with defined structure and bioactivity for cell culture applications are discussed. Finally, a discussion of future directions of engineered protein‐based hydrogels as biomimetic cellular scaffolds is concluded.
Funder
California Institute for Regenerative Medicine
National Science Foundation
Advanced Research Projects Agency for Health
National Heart, Lung, and Blood Institute