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Amelogenin Promotes the Formation of Elongated Apatite Microstructures in a Controlled Crystallization System

机译:Amelogenin促进可控结晶系统中伸长的磷灰石微结构的形成

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摘要

The organic matrix in forming enamel consists largely of the amelogenin protein self-assembled into nanospheres that play a pivotal role in controlling the oriented and elongated growth of highly ordered apatitic crystals during enamel biomineralization. However, the mechanisms of amelogenin-mediated mineralization have not yet been fully elucidated. Here we report that amelogenin dramatically accelerates the nucleation kinetics by decreasing the induction time in a dose-dependent manner in a controlled constant composition (CC) in vitro crystallization system. Remarkably, at very low protein concentrations, elongated microstructures which are similar in appearance to apatitic crystals in enamel were formed at relatively low supersaturations, through interfacial structural match/synergy between structured amelogenin assemblies and apatite nanocrystallites. This heterogeneous crystallization study provides experimental evidence to support the concept that templating by amelogenin very early in the crystallization process facilitates the formation of developing enamel crystals.
机译:形成牙釉质的有机基质主要由自组装成纳米球的牙釉蛋白组成,在釉质生物矿化过程中,该蛋白在控制高度有序的磷灰石晶体的定向和伸长生长中起关键作用。然而,尚未完全阐明釉原蛋白介导的矿化机理。在这里,我们报告在受控恒定成分(CC)体外结晶系统中,成釉蛋白通过以剂量依赖的方式减少诱导时间,从而显着加速成核动力学。值得注意的是,在非常低的蛋白质浓度下,通过结构化的釉质生成蛋白组件和磷灰石纳米微晶之间的界面结构匹配/协同作用,在相对较低的过饱和度下形成了外观与釉质中的脂溶性晶体相似的细长微观结构。这项异质结晶研究提供了实验证据来支持这一概念,即在结晶过程的早期就通过牙釉蛋白进行模板化会促进发育中的牙釉质晶体的形成。

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