Super-Resolution Imaging of Receptor Dynamics and Structure: Self-Association of CEACAM and Its Implications for Cancer,Infection, and Inflammation

受体动力学和结构的超分辨率成像：CEACAM 的自关联及其对癌症、感染和炎症的影响

• 批准号: 255463
• 负责人: Yip Christopher M
• 金额: $ 43.19万
• 依托单位: University of Toronto
• 依托单位国家: 加拿大
• 项目类别: Operating Grants
• 财政年份: 2012
• 资助国家: 加拿大
• 起止时间: 2012-03-01 至 2017-03-01
• 项目状态: 已结题
• 来源: https://webapps.cihr-irsc.gc.ca/decisions/p/project_details.html?applId=255463&lang=en
• 关键词: Fluorescence; Membrane Proteins; Microscopy; Molecular Dynamics; Optical Imaging; Protein-Protein Interactions; Scanning Probe Microscopy; Single Molecule Imaging; Super-Resolution Microscopy

How cells behave and interact is largely determined by interactions between molecules, known as receptors, located on their surface. These interactions are controlled by signals within the cell, through other molecules, and interactions with neighbouring

细胞的行为和相互作用在很大程度上取决于位于其表面的分子（称为受体）之间的相互作用。这些相互作用是由细胞内的信号控制的，通过其他分子，以及与邻近的分子的相互作用。