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Strategic Protein Target Analysis for Developing Drugs to Stop Dental Caries

机译:用于开发可预防龋齿的药物的战略蛋白质靶点分析

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摘要

Dental caries is the most common disease to cause irreversible damage in humans. Several therapeutic agents are available to treat or prevent dental caries, but none besides fluoride has significantly influenced the disease burden globally. Etiologic mechanisms of the mutans group streptococci and specific Lactobacillus species have been characterized to various degrees of detail, from identification of physiologic processes to specific proteins. Here, we analyze the entire Streptococcus mutans proteome for potential drug targets by investigating their uniqueness with respect to non-cariogenic dental plaque bacteria, quality of protein structure models, and the likelihood of finding a drug for the active site. Our results suggest specific targets for rational drug discovery, including 15 known virulence factors, 16 proteins for which crystallographic structures are available, and 84 previously uncharacterized proteins, with various levels of similarity to homologs in dental plaque bacteria. This analysis provides a map to streamline the process of clinical development of effective multispecies pharmacologic interventions for dental caries.
机译:龋齿是引起人类不可逆转损害的最常见疾病。有几种治疗剂可用于治疗或预防龋齿,但除氟化物外,没有一种能显着影响全球的疾病负担。从生理过程的鉴定到特定蛋白质,已对变形菌群链球菌和特定乳杆菌物种的病因机制进行了详细描述。在这里,我们通过研究变形链球菌蛋白质组相对于非致龋性牙菌斑细菌的独特性,蛋白质结构模型的质量以及为该活性位点找到药物的可能性,来分析整个变形链球菌蛋白质组作为潜在药物靶标。我们的研究结果提出了合理药物发现的具体目标,包括15种已知毒力因子,16种具有晶体结构的蛋白质以及84种以前未表征的蛋白质,这些蛋白质与牙菌斑细菌的同源物具有不同程度的相似性。该分析提供了一个地图,可简化对龋齿的有效多物种药理干预措施的临床开发过程。

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