首页> 外文期刊>Biophysical Chemistry: An International Journal Devoted to the Physical Chemistry of Biological Phenomena >AN ANALYSIS OF ANTIGEN-ANTIBODY BINDING KINETICS FOR BIOSENSOR APPLICATIONS UTILIZED AS A MODEL SYSTEM - INFLUENCE OF NON-SPECIFIC BINDING
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AN ANALYSIS OF ANTIGEN-ANTIBODY BINDING KINETICS FOR BIOSENSOR APPLICATIONS UTILIZED AS A MODEL SYSTEM - INFLUENCE OF NON-SPECIFIC BINDING

机译:作为模型系统的生物传感器应用抗原-抗原结合动力学的分析-非特异性结合的影响

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The influence of non-specific binding on the specific binding of antigen in solution to antibody immobilized on a biosensor surface is presented for first-, one and a half-, second-, and other order reactions occurring under external diffusion-limited conditions. Both single step and dual-step binding of antigen to antibody is considered. For a half-order reaction the value of the ratio of non-specific binding to specific binding (alpha) does not affect the rate of specific binding since a single curve represents the binding curve for alpha = 0 to 0.5. An increase in the cu value leads to a decrease in the rare of binding and in the amount of antigen bound specifically to the antibody on the surface for first-, one and a half-, and second-order reactions. Also, an increase in the reaction order increases the sensitivity of the specific binding to the alpha value. An increase in the antigen concentration in solution increases the amount and the rate of specific binding for first-, one and a half-, and second-order reactions. The introduction of non-specific binding leads to complexities in the specific binding of the antigen for the one and half- and second-order reactions as the antibody concentration on the surface is varied. When non-specific binding is present there is an optimum value of the antibody concentration on the surface that yields the maximum rate and amount of antigen specifically bound for one and a half- and second-order reactions. Though this optimum amount of antibody immobilized on the surface is the same for the one and a half-and second-order reactions, it is different for different cu values. No such complexities are observed for first-order reactions. The inclusion of non-specific binding in the analysis provides a more realistic picture of the binding of the antigen in solution to the antibody immobilized on the surface. The figures that show the numerically calculated binding rates for different orders when non-specific binding is present, represent the most useful part of the analysis for readers who are interested in constructing biosensors, and should assist in the control and manipulation of these interactions at the surface. These curves can be used to interpret a far from ideal binding of antigen to an immobilized antibody surface or vice versa. More-or-less all of the analysis should also be applicable to analytical systems that would not be classified as biosensors (that is, immune and receptor assays). [References: 20]
机译:对于在外部扩散限制条件下发生的一级,一级和半级,二级和其他反应,提出了非特异性结合对溶液中抗原与固定在生物传感器表面上的抗体的特异性结合的影响。考虑了抗原与抗体的单步和双步结合。对于半阶反应,非特异性结合与特异性结合的比率(α)的值不影响特异性结合的速率,因为一条曲线代表α= 0至0.5的结合曲线。 cu值的增加导致一阶,一阶,半阶和二阶反应的结合稀有性和与抗体特异性结合的抗原数量减少。同样,反应顺序的增加也增加了特异性结合对α值的敏感性。溶液中抗原浓度的增加增加了一级,一级和半级和二级反应的特异性结合的量和速率。随着表面上抗体浓度的变化,非特异性结合的引入导致针对一阶和半阶和二阶反应的抗原的特异性结合变得复杂。当存在非特异性结合时,在表面上存在抗体浓度的最佳值,该最佳浓度可产生与一阶和半阶和二阶反应特异性结合的抗原的最大速率和最大量。尽管固定在表面上的抗体的最佳量对于一阶和半阶和二阶反应是相同的,但对于不同的cu值却是不同的。对于一阶反应,没有观察到这样的复杂性。分析中包含非特异性结合可提供溶液中抗原与固定在表面上的抗体结合的更真实的图片。这些图显示了存在非特异性结合时不同阶数的数字计算结合率,这些图对于有兴趣构建生物传感器的读者来说,是分析中最有用的部分,应帮助控制和操纵这些相互作用。表面。这些曲线可用于解释抗原与固定抗体表面的理想结合,反之亦然。几乎所有的分析也应适用于不会归类为生物传感器的分析系统(即免疫和受体分析)。 [参考:20]

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