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Measurement of mass transport and reaction parameters in bulk solution using photobleaching. Reaction limited binding regime.

机译:使用光漂白法测量本体溶液中的传质和反应参数。反应受限的结合方案。

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摘要

Fluorescence recovery after photobleaching (FRAP) has been used previously to investigate the kinetics of binding to biological surfaces. The present study adapts and further develops this technique for the quantification of mass transport and reaction parameters in bulk media. The technique's ability to obtain the bulk diffusion coefficient, concentration of binding sites, and equilibrium binding constant for ligand/receptor interactions in the reaction limited binding regime is assessed using the B72.3/TAG-72 monoclonal antibody/tumor associated antigen interaction as a model in vitro system. Measurements were independently verified using fluorometry. The bulk diffusion coefficient, concentration of binding sites and equilibrium binding constant for the system investigated were 6.1 +/- 1.1 x 10(-7) cm2/s, 4.4 +/- 0.6 x 10(-7) M, and 2.5 +/- 1.6 x 10(7) M-1, respectively. Model robustness and the applicability of the technique for in vivo quantification of mass transport and reaction parameters are addressed. With a suitable animal model, it is believed that this technique is capable of quantifying mass transport and reaction parameters in vivo.
机译:以前已经使用光漂白后的荧光恢复(FRAP)来研究与生物表面结合的动力学。本研究适应并进一步发展了这种技术,用于定量分析大体积介质中的传质和反应参数。使用B72.3 / TAG-72单克隆抗体/肿瘤相关抗原相互作用作为技术来评估该技术在反应受限的结合方案中获得配体/受体相互作用的整体扩散系数,结合位点浓度和平衡结合常数的能力。体外系统模型。使用荧光法独立地验证了测量结果。该系统的体积扩散系数,结合位点浓度和平衡结合常数分别为6.1 +/- 1.1 x 10(-7)cm2 / s,4.4 +/- 0.6 x 10(-7)M和2.5 + / -分别为1.6 x 10(7)M-1。提出了模型的稳健性和该技术在体内定量传输质量和反应参数的适用性。对于合适的动物模型,据信该技术能够定量体内的传质和反应参数。

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