Padovano J D, Ravindran S, Snee P T, Ramachandran A, Bedran-Russo A K, George A
Brodie Tooth Development Genetics & Regenerative Medicine Research Laboratory, Department of Oral Biology, University of Illinois at Chicago, Chicago, IL, USA.
Department of Chemistry, College of Liberal Arts and Sciences, University of Illinois at Chicago, Chicago, IL, USA.
J Dent Res. 2015 Apr;94(4):608-14. doi: 10.1177/0022034515572441. Epub 2015 Feb 18.
Remineralization of dentin during dental caries is of considerable clinical interest. Dentin matrix protein 1 (DMP1) is a non-collagenous calcium-binding protein that plays a critical role in biomineralization. In the present study, we tested if peptides derived from DMP1 can be used for dentin remineralization. Peptide pA (pA, MW = 1.726 kDa) and peptide pB (pB, MW = 2.185), containing common collagen-binding domains and unique calcium-binding domains, were synthesized by solid-phase chemistry. An extreme caries lesion scenario was created by collagenase digestion, and the biomineral-nucleating potential of these peptides was ascertained when coated on collagenase-treated dentin matrix and control, native human dentin matrix under physiological levels of calcium and phosphate. Scanning electron microscopy analysis suggests that peptide pB was an effective nucleator when compared with pA. However, a 1:4 ratio of pA to pB was determined to be ideal for dentin remineralization, based on hydroxyapatite (HA) morphology and calcium/phosphorus ratios. Interestingly, HA was nucleated on collagenase-challenged dentin with as little as 20 min of 1:4 peptide incubation. Electron diffraction confirmed the presence of large HA crystals that produced a diffraction pattern indicative of a rod-like crystal structure. These findings suggest that DMP1-derived peptides may be useful to modulate mineral deposition and subsequent formation of HA when exposed to physiological concentrations of calcium and phosphate.
龋病期间牙本质的再矿化具有重要的临床意义。牙本质基质蛋白1(DMP1)是一种非胶原蛋白钙结合蛋白,在生物矿化过程中起关键作用。在本研究中,我们测试了源自DMP1的肽是否可用于牙本质再矿化。通过固相化学合成了含有常见胶原结合域和独特钙结合域的肽pA(pA,分子量 = 1.726 kDa)和肽pB(pB,分子量 = 2.185)。通过胶原酶消化构建了极端龋损情况,并在生理水平的钙和磷酸盐条件下,将这些肽包被在胶原酶处理的牙本质基质和对照天然人牙本质基质上时,确定了它们的生物矿化成核潜力。扫描电子显微镜分析表明,与pA相比,肽pB是一种有效的成核剂。然而,基于羟基磷灰石(HA)形态和钙/磷比率,确定pA与pB的1:4比例对牙本质再矿化是理想的。有趣的是,在1:4肽孵育仅20分钟后,HA就在胶原酶处理的牙本质上成核。电子衍射证实存在大的HA晶体,其产生的衍射图案表明为棒状晶体结构。这些发现表明,当暴露于生理浓度的钙和磷酸盐时,源自DMP1的肽可能有助于调节矿物质沉积和随后HA的形成。