Shlaferman Jacob, Paige Alexander, Meserve Krista, Miech Jason A, Gerdon Aren E
Department of Chemistry and Physics, Emmanuel College, 400 The Fenway, Boston, Massachusetts 02115, United States.
ACS Biomater Sci Eng. 2019 Jul 8;5(7):3228-3236. doi: 10.1021/acsbiomaterials.9b00308. Epub 2019 Jun 25.
DNA aptamers previously selected as calcium phosphate mineralization templates were modified and analyzed to better understand structure-function relationships and to explore the mechanism of templated mineralization. Aptamers were created to strengthen or remove a prevalent G-quadruplex structure and were analyzed for structural stability, affinity to calcium phosphate, influence on homogeneous and heterogeneous calcium phosphate mineralization, and influence on mineral crystallinity and morphology. Aptamers were found to modulate mineralization kinetics in a concentration-dependent manner. Changes to the G-quadruplex structure affected affinity to hydroxyapatite (Ca(PO)(OH), HAP) and had a substantial impact on the mineral crystallinity. We propose a model for aptamer-directed mineralization and anticipate the usefulness of these aptamer sequences in future biomimetic and biomedical applications.
先前被选作磷酸钙矿化模板的DNA适配体经过修饰和分析,以更好地理解结构-功能关系,并探索模板矿化的机制。构建了用于增强或去除普遍存在的G-四链体结构的适配体,并对其结构稳定性、对磷酸钙的亲和力、对均相和异相磷酸钙矿化的影响以及对矿物结晶度和形态的影响进行了分析。发现适配体以浓度依赖的方式调节矿化动力学。G-四链体结构的改变影响了对羟基磷灰石(Ca(PO)(OH),HAP)的亲和力,并对矿物结晶度产生了重大影响。我们提出了一个适配体导向矿化的模型,并预期这些适配体序列在未来的仿生和生物医学应用中的实用性。