Development of Biodiagnostic Devices Based on Differential Adhesion Under Flow

基于流动下粘附力差异的生物诊断装置的开发

• 批准号: 9986384
• 负责人: Daniel Hammer
• 金额: $ 38.21万
• 依托单位: University of Pennsylvania
• 依托单位国家: 美国
• 项目类别: Continuing Grant
• 财政年份: 2000
• 资助国家: 美国
• 起止时间: 2000-09-15 至 2003-12-31
• 项目状态: 已结题
• 来源: https://www.nsf.gov/awardsearch/showAward?AWD_ID=9986384&HistoricalAwards=false
• 关键词: Development; Biodiagnostic; Devices; Based; Differential

The objective of this project is to develop and quantify methods that employ differential cell adhesion to isolate cells, with the primary goal being to identify cell subpopulations based on the chemistry of their surface receptor. Using three different surfaces (polyacrylamide gels, alkanethiols, or glass slides), micropatterned arrays of ligands will be made. An arrayer will be used to make micropatterned surfaces. The surfaces will be derivatized with antigens or avidin, which will allow the surface to capture cells bearing antibodies (RBL cells) or Biotin (KG1a cells). The adhesion will be measured by optical videomicroscopy, and the yield and selectivity of the binding, as well as the rate constant of cell adhesion, will be measured as a function of cell surface molecular density, substrate ligand density, recognition kinetics and affinity, shear rate, and micropattern geometry. Both model systems (to assess fundamental relationships) and a system of practical interest (the isolation of a stem cell line) will be explored. These experiments will be modeled using a simulation algorithm that has the potential.

该项目的目的是开发和量化采用差分细胞粘附来分离细胞的方法，其主要目标是基于其表面受体的化学性质鉴定细胞亚群。 使用三种不同的表面（聚丙烯酰胺凝胶，烷烃或载玻片），将制成微图案的配体阵列。 阵列将用于制作微图案表面。 表面将用抗原或抗原素衍生化，这将使表面捕获带有抗体（RBL细胞）或生物素（Kg1a细胞）的细胞。 粘附将通过光学视频显微镜检查测量，结合的产率和选择性以及细胞粘附的速率常数将以细胞表面分子密度，底物配体密度，识别动力学和亲和力，剪切速率和microPattern seemetry的函数来测量。 两个模型系统（评估基本关系）和实际关注系统（干细胞系的隔离）将被探索。 这些实验将使用具有潜力的模拟算法进行建模。