釉原蛋白
无定形磷酸钙
搪瓷漆
化学
钙
磷酸盐
透射电子显微镜
矿化(土壤科学)
生物物理学
磷灰石
牙釉质
生物矿化
傅里叶变换红外光谱
结晶学
化学工程
矿物学
生物化学
材料科学
纳米技术
有机化学
生物
复合材料
工程类
基因
氮气
作者
Seo‐Young Kwak,Samantha Green,Felicitas B. Bidlack,Elia Beniash,Yasuo Yamakoshi,James P. Simmer,H.C. Margolis
标识
DOI:10.1111/j.1600-0722.2011.00911.x
摘要
Amelogenin is essential for proper enamel formation. The present in vitro study extends our previous work at low (10 mM) ionic strength (IS) by examining the effect of amelogenin on mineralization under higher (162 mM) IS conditions found in developing enamel. Full-length phosphorylated (P173) and non-phosphorylated (rP172) amelogenins were examined, along with P148 and rP147 that lack the hydrophilic C-terminus. Calcium phosphate formation was assessed by pH change, while the minerals formed were characterized using transmission electron microscopy (TEM) and Fourier transform infrared spectroscopy. Amelogenin self-assembly was also studied using dynamic light scattering and TEM. The results indicate that IS does not influence the effects of rP147, rP172, and P173 on mineralization. However, in contrast to the findings for low IS, where both P173 and P148 stabilize initially formed amorphous calcium phosphate (ACP) nanoparticles for >1 d, elongated hydroxyapatite crystals were observed after 24 h using P148 at high IS, unlike that seen with P173. Differences in self-assembly help explain these findings, which suggest that P173 and P148 may play different roles in regulating enamel mineral formation. The present data support the notion that proteolytic processing of P173 is required in vivo to induce the transformation of initial ACP phases to apatitic enamel crystals.
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