Department of Mechanical Engineering, The University of Texas at Dallas, 800 West Campbell Road, Richardson, Texas 75080, United States.
College of Material and Textile Engineering, Jiaxing University, Jiaxing 314001, People's Republic of China.
ACS Appl Mater Interfaces. 2020 Jun 3;12(22):25363-25373. doi: 10.1021/acsami.0c01613. Epub 2020 May 21.
The noncollagenous interfibrillar interface in bone provides the critical function of transferring loads among collagen fibrils and their bundles, with adhesive mechanisms at this site thus significantly contributing to the mechanical properties of bone. Motivated by the experimental observations and hypotheses, a computational study is presented to elucidate the critical roles of two major proteins at the nanoscale interfibrillar interface, that is, osteopontin (OPN) and osteocalcin (OC) in bone. This study reveals the extremely high interfacial toughness of the OPN/OC composite. The previously proposed hypothesis of sacrificial bonds in the extracellular organic matrix is tested, and the remarkable mechanical properties of the nanoscale bone interface are attributed to the collaborative interactions between the OPN and OC proteins.
骨中非胶原蛋白纤维间界面提供了在胶原纤维及其束之间传递载荷的关键功能,该界面的黏附机制因此对骨的机械性能有重要贡献。受实验观察和假说的启发,本文进行了一项计算研究,以阐明骨中两种主要的纳米级纤维间界面蛋白(即骨桥蛋白(OPN)和骨钙素(OC))的关键作用。本研究揭示了 OPN/OC 复合材料极高的界面韧性。对细胞外有机基质中牺牲键假说进行了检验,纳米级骨界面的优异力学性能归因于 OPN 和 OC 蛋白之间的协同相互作用。