Molecular co-assembled strategy tuning protein conformation for cartilage regeneration.
Chengkun ZhaoXing LiXiaowen HanZhulian LiShaoquan BianWeinan ZengMingming DingJie LiangQing JiangZong-Ke ZhouYujiang FanXingdong ZhangYong SunPublished in: Nature communications (2024)
The assembly of oligopeptide and polypeptide molecules can reconstruct various ordered advanced structures through intermolecular interactions to achieve protein-like biofunction. Here, we develop a "molecular velcro"-inspired peptide and gelatin co-assembly strategy, in which amphiphilic supramolecular tripeptides are attached to the molecular chain of gelatin methacryloyl via intra-/intermolecular interactions. We perform molecular docking and dynamics simulations to demonstrate the feasibility of this strategy and reveal the advanced structural transition of the co-assembled hydrogel, which brings more ordered β-sheet content and 10-fold or more compressive strength improvement. We conduct transcriptome analysis to reveal the role of co-assembled hydrogel in promoting cell proliferation and chondrogenic differentiation. Subcutaneous implantation evaluation confirms considerably reduced inflammatory responses and immunogenicity in comparison with type I collagen. We demonstrate that bone mesenchymal stem cells-laden co-assembled hydrogel can be stably fixed in rabbit knee joint defects by photocuring, which significantly facilitates hyaline cartilage regeneration after three months. This co-assembly strategy provides an approach for developing cartilage regenerative biomaterials.
Keyphrases
- tissue engineering
- mesenchymal stem cells
- molecular docking
- hyaluronic acid
- stem cells
- wound healing
- cell proliferation
- drug delivery
- bone regeneration
- molecular dynamics simulations
- extracellular matrix
- umbilical cord
- genome wide
- single molecule
- energy transfer
- cell therapy
- protein protein
- bone marrow
- cell cycle
- binding protein
- bone mineral density
- postmenopausal women