Basiri T, Johnson N D, Moffa E B, Mulyar Y, Serra Nunes P L, Machado M A A M, Siqueira W L
1 School of Dentistry and Department of Biochemistry, Schulich School of Medicine & Dentistry, The University of Western Ontario, London, ON, Canada.
2 Department of Pediatric Dentistry, Orthodontics and Public Health, Bauru Dental School, University of São Paulo, Bauru, Brazil.
J Dent Res. 2017 Sep;96(10):1162-1167. doi: 10.1177/0022034517708552. Epub 2017 May 16.
Proteins that have existed for millions of years frequently contain repeats of functional domains within their primary structure, thereby improving their functional capacity. In the evolutionary young statherin protein contained within the in vivo-acquired enamel pellicle (AEP), we identified a single functional domain (DR9) located within the protein N-terminal portion that exhibits a higher affinity for hydroxyapatite and more efficient protection against enamel demineralization compared to other native statherin peptides. Thus, we tested the hypothesis that multiplication of functional domains of naturally occurring pellicle peptides amplifies protection against enamel demineralization. In addition, a specific amino acid sequence from histatin 3 (RR-14) was introduced to the hybrid peptides for further testing. Enamel specimens were sectioned to 150-µm thickness and randomly grouped as follows: DR9, DR9-DR9, DR9-RR14, statherin, histatin 1, or distilled water (control). After submersion for 2 h at 37°C, the specimens were placed in 2 mL demineralization solution for 12 d at 37°C. Upon sample removal, the remaining solution was subjected to colorimetric assays to determine the amount of calcium and phosphate released from each specimen. DR9-DR9 amplified protection against enamel demineralization when compared to single DR9 or statherin. Notably, the hybrid peptide DR9-RR14 demonstrated relatively strong protection when the antimicrobial property of these peptides was tested against Candida albicans and Streptococcus mutans. DR9-RR14 was able to maintain 50% of the antifungal activity compared with RR14 for C. albicans and similar values of S. mutans killing activity. This study has pioneered the functional exploration of the natural peptide constituents of the AEP and their evolution-inspired engineered peptides. The knowledge obtained here may provide a basis for the development of stable (proteinase-resistant) synthetic peptides for therapeutic use against dental caries, dental erosion, and/or oral candidiasis.
存在数百万年的蛋白质在其一级结构中常常包含功能域重复序列,从而提高其功能能力。在体内获得性牙釉质薄膜(AEP)中含有的进化上较年轻的组蛋白(statherin)蛋白中,我们在该蛋白的N端部分鉴定出一个单一功能域(DR9),与其他天然组蛋白肽相比,它对羟基磷灰石具有更高的亲和力,并且对牙釉质脱矿具有更有效的保护作用。因此,我们测试了这样一个假设:天然存在的牙釉质薄膜肽的功能域倍增会增强对牙釉质脱矿的保护作用。此外,将来自富组蛋白3(RR - 14)的特定氨基酸序列引入杂交肽中进行进一步测试。将牙釉质标本切成150微米厚,并随机分组如下:DR9、DR9 - DR9、DR9 - RR14、组蛋白、富组蛋白1或蒸馏水(对照)。在37°C下浸泡2小时后,将标本置于2毫升脱矿溶液中,在37°C下放置12天。取出样品后,对剩余溶液进行比色测定,以确定每个标本释放的钙和磷的量。与单个DR9或组蛋白相比,DR9 - DR9增强了对牙釉质脱矿的保护作用。值得注意的是,当测试这些肽对白色念珠菌和变形链球菌的抗菌性能时,杂交肽DR9 - RR14表现出相对较强的保护作用。与RR14相比,DR9 - RR14对白色念珠菌能够保持50%的抗真菌活性,对变形链球菌的杀菌活性值相似。本研究率先对AEP的天然肽成分及其受进化启发的工程肽进行了功能探索。在此获得的知识可为开发用于治疗龋齿、牙侵蚀和/或口腔念珠菌病的稳定(抗蛋白酶)合成肽提供依据。