Measuring Receptor-Ligand Binding Kinetics on Cell Surfaces: From Adhesion Frequency to Thermal Fluctuation Methods

被引:69
作者
Chen, Wei [2 ]
Zarnitsyna, Veronika I. [1 ]
Sarangapani, Krishna K. [1 ,2 ]
Huang, Jun [1 ]
Zhu, Cheng [1 ,2 ]
机构
[1] Georgia Inst Technol, Coulter Dept Biomed Engn, Atlanta, GA 30332 USA
[2] Georgia Inst Technol, George W Woodruff Sch Mech Engn, Atlanta, GA 30332 USA
基金
美国国家卫生研究院;
关键词
Adhesion frequency assay; Thermal fluctuation assay; Micropipette; Biomembrane force probe; Kinetics; Receptor-ligand interaction;
D O I
10.1007/s12195-008-0024-8
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Interactions between surface-anchored receptors and ligands mediate cell-cell and cell-environment communications in many biological processes. Molecular interactions across two apposing cell membrane are governed by two-dimensional (2D) kinetics, which are physically distinct from and biologically more relevant than three-dimensional (3D) kinetics with at least one interacting molecular species in the. fluid phase. Here we review two assays for measuring 2D binding kinetics: the adhesion frequency assay and the thermal. fluctuation assay. The former measures the binding frequency as a function of contact duration and extracts the force-free 2D kinetics parameters by nonlinearly. fitting the data with a probabilistic model. The latter detects bond formation/dissociation by monitoring the reduction/resumption of thermal. fluctuations of a force sensor. Both assays are mechanically based and operate at the level of mostly single molecular interaction, which requires ultrasensitive force techniques. Characterization of one such technique, the biomembrane force probe, is presented.
引用
收藏
页码:276 / 288
页数:13
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