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酶促人工骨矿物质模板化

Enzyme Directed Templating of Artificial Bone Mineral.

作者信息

Spoerke Erik D, Anthony Shawn G, Stupp Samuel I

机构信息

Department of Materials Science and Engineering, Northwestern University, Evanston, IL USA.

出版信息

Adv Mater. 2009 Jan 26;21(4):425-430. doi: 10.1002/adma.200802242.

DOI:10.1002/adma.200802242
PMID:22068437
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3075609/
Abstract

Bone is one of Nature's most remarkable materials, not only for its mechanical properties but also for its ability to repair fractures and remodel its microstructure in response to stress. At the nanoscale bone is a supramolecular matrix of collagen fibers reinforced by hydroxyapatite crystals with a high degree of order. Emulating elements of the biological synthesis of this composite could help develop strategies for advanced materials. Previous work has demonstrated the use of functionalized peptide amphiphile nanofibers in a two-dimensional system to emulate hydroxyapatite mineralization in natural bone. We describe here an artificial, in vitro biomineralization process that allows a similar process to occur in three dimensions. The system employs the natural enzyme alkaline phosphatase and a phosphorylated, anionic nanofiber gel matrix to template hydroxyapatite nanocrystals with size, shape, and crystallographic orientation resembling natural bone mineral. The formation of this biomimetic mineral in three dimensions results from the synergy of fiber-induced nucleation and the temporal control of phosphate ion harvesting by the enzyme. Gradual enzymatic harvesting of ions for crystal growth and the strong nucleating ability of the phosphorylated fibers suppresses uncontrolled precipitation of mineral. The strategy could lead to biomimetic materials to promote bone regeneration or the synthesis of hybrid materials with crystallographically defined structures.

摘要

骨骼是自然界最非凡的物质之一,不仅因其力学性能,还因其修复骨折以及响应应力重塑其微观结构的能力。在纳米尺度上,骨骼是由羟基磷灰石晶体增强的胶原纤维超分子基质,具有高度的有序性。模拟这种复合材料生物合成的元素有助于开发先进材料的策略。先前的工作已经证明了在二维系统中使用功能化肽两亲性纳米纤维来模拟天然骨骼中的羟基磷灰石矿化。我们在此描述一种人工体外生物矿化过程,该过程允许在三维空间中发生类似的过程。该系统利用天然酶碱性磷酸酶和磷酸化的阴离子纳米纤维凝胶基质来模板化尺寸、形状和晶体取向类似于天然骨矿物质的羟基磷灰石纳米晶体。这种三维仿生矿物质的形成源于纤维诱导成核与酶对磷酸根离子捕获的时间控制之间的协同作用。酶对离子的逐步捕获用于晶体生长以及磷酸化纤维的强成核能力抑制了矿物质的无控制沉淀。该策略可能会产生促进骨再生的仿生材料或具有晶体学定义结构的杂化材料的合成。