脚手架
寡肽
脐静脉
肽
间充质干细胞
化学
细胞生物学
再生(生物学)
骨髓
生物医学工程
钙
组织工程
生物物理学
人骨
骨愈合
自组装肽
血管生成
材料科学
干细胞
生物化学
内皮干细胞
再生医学
骨组织
骨生长
生长因子
作者
Shiqing Ma,Xiaotong Liu,Baichuan Xiao,YiFan Xiao,Yilin Yang,Beibei Ma,Yucheng Shang,Hao Zhu,Yixiang Zhou,Yong‐Biao Zhang,Jiayin Deng
标识
DOI:10.1002/adhm.202505458
摘要
Bone defects caused by inflammation, trauma, tumor resection, or tooth extraction present persistent clinical challenges, primarily because of the limitations of current bone graft materials and growth factor therapies. In this study, we developed a novel strategy for bone regeneration by integrating AI-driven peptide discovery with bone tissue engineering. Utilizing the Deepeptide platform, we screened and identified bifunctional oligopeptides from intrinsically disordered regions (IDRs) with both osteogenic and angiogenic activities. Among the nine candidates, the most potent peptide was fused with a hydroxyapatite-binding domain via peptide engineering to enhance scaffold coupling and achieve sustained release. The recombinant fusion peptide was then covalently anchored onto biphasic calcium phosphate (BCP) ceramic scaffolds. And evaluations demonstrated that the modified scaffolds significantly promoted osteogenic differentiation of bone marrow mesenchymal stem cells (BMSCs), angiogenic activity of human umbilical vein endothelial cells (HUVECs), and effective bone regeneration and vascularization in vivo. These findings suggest that AI-discovered, functionally integrated oligopeptide-modified BCP ceramics hold promise as next-generation bone graft for repairing critical-sized bone defects.
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