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用于生物传感器应用的分析物-受体结合动力学分析:分形维数对结合速率系数的影响。

An analysis of analyte-receptor binding kinetics for biosensor applications: influence of the fractal dimension on the binding rate coefficient.

作者信息

Sadana A

机构信息

Chemical Engineering Department, University of Mississippi 38677-9740, USA.

出版信息

Biosens Bioelectron. 1998 Nov 1;13(10):1127-40. doi: 10.1016/s0956-5663(98)00005-0.

Abstract

The diffusion-limited binding kinetics of analyte in solution to receptor immobilized on a biosensor surface is analysed within a fractal framework. Both a single- as well as a dual-fractal analysis are utilized. Antigen-antibody and analyte-receptor systems are analysed. For the antigen-antibody and analyte-receptor systems where a single- or a dual-fractal analysis was used, it is of interest to note that the binding rate coefficient and the fractal dimension exhibit changes in the same direction. The binding rate coefficient expressions obtained as a function of the fractal dimension indicate the high sensitivity of the binding rate coefficient with respect to the fractal dimension. For example, for a single-fractal analysis and for the binding of (a) 1 microM BSA in solution to the anti-BSA-protein fused to a biosensor surface, and for (b) the binding of m-xylene-saturated STE buffer solution to the microorganism immobilized to the fiber-optic end and covered with a polycarbonate membrane, the orders of dependence of the binding rate coefficient on the fractal dimension were 5.535 and 3.314, respectively. This emphasizes the importance of the degree of heterogeneity on the biosensor surface and its impact on the binding rate coefficient, k. This high sensitivity is also indicated for a dual-fractal analysis, at least for the binding rate coefficient, k2. For example, during regeneration runs and for the binding of polymerase chain-reaction amplified DNA in solution to DNA capture protein immobilized on a fiber-optic biosensor, the order of dependence of k2 on Df2 was 3.399. The fractional order of dependence of the binding rate coefficient(s) on the fractal dimension(s) further reinforces the fractal nature of the system. The binding rate coefficient expressions developed as a function of the fractal dimension for both single-fractal analysis and dual-fractal analysis systems are of particular value since they provide a means to better control biosensor performance by linking it to the heterogeneity on the surface. Also, the importance of the nature of the surface on biosensor performance is emphasized in a quantitative sense.

摘要

在分形框架内分析了溶液中分析物与固定在生物传感器表面的受体之间的扩散限制结合动力学。采用了单分形和双分形分析。对抗抗原-抗体和分析物-受体系统进行了分析。对于使用单分形或双分形分析的抗原-抗体和分析物-受体系统,值得注意的是结合速率系数和分形维数在相同方向上呈现变化。作为分形维数函数获得的结合速率系数表达式表明结合速率系数相对于分形维数具有高灵敏度。例如,对于单分形分析以及(a)溶液中1 microM牛血清白蛋白与融合到生物传感器表面的抗牛血清白蛋白蛋白的结合,以及(b)间二甲苯饱和的STE缓冲溶液与固定在光纤末端并覆盖有聚碳酸酯膜的微生物的结合,结合速率系数对分形维数的依赖阶数分别为5.535和3.314。这强调了生物传感器表面异质性程度及其对结合速率系数k的影响的重要性。对于双分形分析,至少对于结合速率系数k2,也表明了这种高灵敏度。例如,在再生运行期间以及溶液中聚合酶链反应扩增的DNA与固定在光纤生物传感器上的DNA捕获蛋白的结合过程中,k2对Df2的依赖阶数为3.399。结合速率系数对分形维数的分数依赖阶数进一步强化了系统的分形性质。为单分形分析和双分形分析系统开发的作为分形维数函数的结合速率系数表达式具有特别的价值,因为它们提供了一种通过将生物传感器性能与表面异质性联系起来更好地控制生物传感器性能的方法。此外,从定量意义上强调了表面性质对生物传感器性能的重要性。

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