免疫应答所需的表面受体相互作用动力学

V. K. Thomas, Jianhua Wu, C. Zhu, Michael Loran Dustin
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引用次数: 0

摘要

我们提出了一种测量二维动力学速率的新方法来研究免疫应答调节中重要受体之间的相互作用。分化簇(cd28)与CD80的相互作用刺激T细胞活化,而细胞毒性T淋巴细胞抗原(CTLA)-4与CD80的相互作用是T细胞活化的拮抗剂。新的分析提供了有关自由配体在接触区域的扩散,稳定的相互作用的比例和动力学偏离率的信息。从平衡测量的独立数据被用来计算接通率。CD28-CD80相互作用的值显示自由CD80扩散减少了10倍,稳定分数为9.6%,2D k/sub r/为0.057 s/sup -1/。这与1.6 s/sup -1/ in溶液的中断率相比,相差30倍。CTLA-4-CD28系统正在分析中,但似乎具有较慢的动力学,需要很长的恢复时间才能进行分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dynamics of surface receptor interactions required for an immune response
We have applied a new method for measuring two dimensional kinetic rates to the study the interactions between receptor important for the regulation of the immune response. The interaction of Cluster of Differentiation (CD) 28 with CD80 stimulates T cell activation, while the interaction of Cytotoxic T Lymphocyte Antigen (CTLA)-4 with CD80 is an antagonist to T cell activation. The new analysis provides information about free ligand diffusion in the contact area, the fraction of interactions that are stable and the kinetic off-rate. Independent data from equilibrium measurements are used to calculate the on-rate. The values for CD28-CD80 interaction reveal a 10-fold reduction in free CD80 diffusion, a small stable fraction of 9.6% and a 2D k/sub r/ of 0.057 s/sup -1/. This compares to an off-rate of 1.6 s/sup -1/ in solution, a difference of 30-fold. The CTLA-4-CD28 system is under analysis, but appears to have slower kinetics, requiring very long recovery time courses for analysis.
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