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Quantification of transport and binding parameters using fluorescence recovery after photobleaching. Potential for in vivo applications.

机译:使用光漂白后的荧光回收定量运输和结合参数。体内应用的潜力。

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摘要

Fluorescence Recovery After Photobleaching (FRAP) has been used extensively in the study of transport and binding in biological media in vitro. The present study adapts and further develops FRAP so that it may be utilized for the in vivo quantification of binding parameters. The technique is validated in vitro by measuring mass transport and binding parameters for the Concanavalin A/Mannose binding system (a diffusion-limited system). The pseudo-equilibrium constant (the product of the equilibrium constant and the total concentration of binding sites) for this system was determined to be 26 +/- 15 which compares favorably with literature values ranging between 16 and 32. The applicability of this technique to measure parameters for monoclonal antibody/antigen interactions in a thin tissue preparation such as the rabbit ear chamber tissue preparation is also examined. Unlike other methods for measuring binding parameters, this is the only technique which has the potential to measure parameters relevant to antibody delivery in vivo. The proposed technique is noninvasive and does not require a priori knowledge of, independent measurement of, or variation in the concentration of binding sites or total concentration of binding species.
机译:光漂白后的荧光恢复(FRAP)已广泛用于体外生物介质中的运输和结合研究。本研究适应并进一步开发了FRAP,因此可用于体内结合参数的定量。通过测量伴刀豆球蛋白A /甘露糖结合系统(扩散受限系统)的传质和结合参数,对该技术进行了体外验证。该系统的拟平衡平衡常数(平衡常数与结合位点总浓度的乘积)确定为26 +/- 15,与文献值16至32相比具有优势。还检查了薄组织制剂(如兔耳腔组织制剂)中单克隆抗体/抗原相互作用的测量参数。与其他用于测量结合参数的方法不同,这是唯一一种可以测量与体内抗体传递相关的参数的技术。所提出的技术是非侵入性的,不需要先验知识,对结合位点的浓度或结合种类的总浓度的独立测量或变化。

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