Center for Craniofacial Molecular Biology, University of Southern California, Herman Ostrow School of Dentistry, 2250 Alcazar St., Los Angeles, CA 90033, USA.
J Struct Biol. 2011 Nov;176(2):220-8. doi: 10.1016/j.jsb.2011.07.016. Epub 2011 Aug 5.
Amelogenin is cleaved by enamelysin (Mmp-20) soon after its secretion, and the cleavage products accumulate in specific locations during enamel formation, suggesting that parent amelogenin proteolysis is necessary for activating its functions. To investigate the precise roles of Mmp-20 and its influence on the assembly of amelogenin, an in vitro enzymatic digestion process mimicking the initial stages of amelogenin proteolysis was investigated at near-physiological conditions using recombinant porcine amelogenin (rP172) and enamelysin. Hierarchically organized nanorod structures formed during different digestion stages were detected by TEM. At the earliest stage, uniformly dispersed parent amelogenin spherical particles, mixed with some darker stained smaller spheres, and accompanying elongated chain-like nanostructures were observed. Cylindrical nanorods, which appeared to be the result of tight assembly of thin subunit cylindrical discs with thicknesses ranging from ∼2.5 to ∼6.0nm, were formed after an hour of proteolysis. These subunit building blocks stacked to form nanorods with maximum length of ∼100nm. With the production of more cleavage products, additional morphologies spontaneously evolved from the cylindrical nanorods. Larger ball-like aggregates ultimately formed at the end of proteolysis. The uniform spherical particles, nanorods, morphological patterns evolved from nanorods, and globular aggregated microstructures were successively formed by means of co-assembly of amelogenin and its cleavage products during a comparatively slow proteolysis process. We propose that, following the C-terminal cleavage of amelogenin, co-assembly with its fragments leads to formation of nanorod structures whose properties eventually dictate the super-structural organization of enamel matrix, controlling the elongated growth of enamel apatite crystals.
釉原蛋白在分泌后不久就被釉原蛋白酶(Mmp-20)切割,其切割产物在釉质形成过程中积累在特定位置,这表明亲本釉原蛋白的蛋白水解对于激活其功能是必要的。为了研究 Mmp-20 的精确作用及其对釉原蛋白组装的影响,在接近生理条件下,使用重组猪釉原蛋白(rP172)和釉原蛋白酶模拟釉原蛋白初始阶段的酶解过程进行了体外酶消化实验。通过 TEM 检测到不同消化阶段形成的分级排列纳米棒结构。在最早的阶段,观察到均匀分散的亲本釉原蛋白球形颗粒,与一些较暗染色的较小球体混合,并伴有拉长的链状纳米结构。在 1 小时的蛋白水解后,形成了圆柱形纳米棒,其似乎是由厚度在 2.5 至 6.0nm 之间的薄亚单位圆柱形盘的紧密组装形成的。这些亚单位构建块堆积在一起,形成了最长约 100nm 的纳米棒。随着更多切割产物的产生,从圆柱形纳米棒中自发演化出更多的形态。在蛋白水解结束时,最终形成了更大的球状聚集体。在相对缓慢的蛋白水解过程中,釉原蛋白及其切割产物通过共组装连续形成均匀的球形颗粒、纳米棒、由纳米棒演化而来的形态模式以及球形聚集的微观结构。我们提出,在釉原蛋白的 C 端切割之后,与片段的共组装导致纳米棒结构的形成,其性质最终决定了釉基质的超结构组织,控制着釉质磷灰石晶体的拉长生长。