STRUCTURAL BIOLOGY OF THE ENAMEL PROTEINS

牙釉质蛋白质的结构生物学

• 批准号: 8169739
• 负责人: Janet M. Oldak
• 金额: $ 0.18万
• 依托单位: UNIVERSITY OF CALIFORNIA, SAN FRANCISCO
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-09-12 至 2011-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8169739
• 关键词: Apatites; Architecture; Area; Binding; Biomimetics; Computer Retrieval of Information on Scientific Projects Database; Dental Enamel; Development; Extracellular Matrix; Funding; Future; Gel; Goals; Grant; Growth; In Vitro; Institution; Lead; MMP-20; Minerals; Molecular; Morphology; Nanosphere; Nature; Peptide Hydrolases; Proteins; Research; Research Activity; Research Personnel; Resources; Solutions; Source; Structure; United States National Institutes of Health; amelogenin; base; octacalcium phosphate; self assembly; structural biology

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. The major goal of our research activities is to advance our understanding of the fundamental molecular mechanisms involved in the formation of dental enamel. We postulate that such understanding will lead to the future development of biomimetic strategies for the creation of enamel-like mineral materials. We focus on two areas: 1. The structure and function of enamel extracellular matrix components. 2) The function and mechanism of action of enamel proteinases MMP-20 and KLK-4. Our goals are: ( project #1) to identify the nature of the interactions which define protein self-assembly in solution and the nanosphere matrix architecture, at the molecular level, to define at the molecular level the ultrastructural architecture of amelogenin-based matrices formed in vitro, to characterize apatite and octacalcium phosphate crystal growth, morphology and orientation within synthetic amelogenin gel matrices in the absence and presence of the non-amelogenins. (project # 2) : To investigate the function of MMP-20 in the assembly, dis-assembly and apatite binding of amelogenin and its proteolytic products.

这个子项目是许多研究子项目中的一个 由NIH/NCRR资助的中心赠款提供的资源。子项目和 研究者（PI）可能从另一个NIH来源获得了主要资金， 因此可以在其他CRISP条目中表示。所列机构为 研究中心，而研究中心不一定是研究者所在的机构。 我们研究活动的主要目标是促进我们对牙釉质形成的基本分子机制的理解。我们假设，这种理解将导致未来的发展仿生策略创造搪瓷类矿物材料。我们专注于两个领域：1。釉质细胞外基质成分的结构与功能。2)釉蛋白酶MMP-20和KLK-4的功能和作用机制。我们的目标是：（项目#1）在分子水平上鉴定限定蛋白质在溶液中自组装和纳米球基质结构的相互作用的性质，在分子水平上限定体外形成的基于釉原蛋白的基质的超微结构，表征磷灰石和磷酸八钙晶体生长，在不存在和存在非釉原蛋白的情况下，在合成的釉原蛋白凝胶基质中的形态和取向。（项目#2）：研究MMP-20在釉原蛋白及其蛋白水解产物的组装、解聚和磷灰石结合中的功能。