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Novel surface energy sensor for detecting protein adsorption and subsequent conformation change.

机译:新型表面能传感器,用于检测蛋白质吸附和随后的构象变化。

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This thesis describes the development of a novel experimental technique to measure the change in surface energy of a sensing membrane as molecules adsorb to its surface. The sensor is constructed from a thin elastomeric membrane mounted on an annular support that is immersed in an aqueous solution. The sensor is acoustically actuated to resonate in a selected mode of oscillation and the change of resonant frequency of the sensor as a function of time is monitored. These sensing membranes have a low inherent tension such that the surface energy on its two interfaces dominate the membrane tension and the adsorption of molecules decreases the surface energy and thus reduces the resonant frequency of the membrane.; The adsorption behaviour of two types of molecules were investigated; surfactants and proteins. While the sensor responds quickly (∼1--2 minutes) to the adsorption of the small surfactant molecules, it exhibits a long time response over many hours to the adsorption of protein molecules. This long time response is attributed to the slow conformation change of the protein molecules once they have adsorbed. An auxiliary method to measure the amount of protein molecules on the surface of the membrane was devised to run simultaneously with the observations of resonant frequency. This technique employed fluorescent excitation of tagged protein molecules in an optical evanescent field. This measurement confirmed that the population of protein molecules on the surface did indeed reach a steady-state value within 30 minutes, in turn confirming the sensitivity of the sensing membrane to molecular conformation change.; A step-wise kinetic protein adsorption model was developed and compared to the experimental data generated in the simultaneous measurement described above. This model was able to successfully describe the puzzling kinetics of protein adsorption to, and desorption from, the sensing membrane. This required a key, non-obvious term in the rate equations---the molecules in the bulk solution are found to make an important contribution to both the desorption of bound molecules and also their slow conformation change. This observation provides an effective and self-consistent explanation for the previously conflicting notions of adsorption isotherms and irreversibility.
机译:本文描述了一种新的实验技术的发展,该技术用于测量当分子吸附到传感膜表面时传感膜表面能的变化。传感器由弹性薄膜制成,该弹性薄膜安装在浸入水溶液中的环形支架上。传感器被声学促动以在选定的振荡模式下谐振,并且监测传感器的谐振频率随时间的变化。这些传感膜具有低的固有张力,使得其两个界面上的表面能支配着膜的张力,分子的吸附降低了表面能,从而降低了膜的共振频率。研究了两种分子的吸附行为。表面活性剂和蛋白质。尽管传感器对表面活性剂小分子的吸附反应迅速(约1--2分钟),但在数小时内却对蛋白质分子的吸附表现出长时间响应。这种长时间的响应归因于蛋白质分子一旦被吸附,其构象变化缓慢。设计了一种辅助方法来测量膜表面蛋白质分子的数量,以便与共振频率的观测同时进行。该技术在渐逝光场中采用了标记蛋白分子的荧光激发。该测量结果证实了表面上蛋白质分子的确确实在30分钟内达到了稳态值,进而证实了传感膜对分子构象变化的敏感性。建立了逐步的动力学蛋白质吸附模型,并将其与在上述同时测量中生成的实验数据进行了比较。该模型能够成功地描述蛋白质吸附到传感膜和从传感膜解吸的令人费解的动力学。这在速率方程中需要一个关键的,非显而易见的术语-本体溶液中的分子被发现对结合分子的解吸及其缓慢的构象变化都起着重要的作用。该观察结果为先前相互矛盾的吸附等温线和不可逆性概念提供了有效且自洽的解释。

著录项

  • 作者

    Clark, Alison Jane.;

  • 作者单位

    The University of British Columbia (Canada).;

  • 授予单位 The University of British Columbia (Canada).;
  • 学科 Engineering Biomedical.; Biophysics General.
  • 学位 Ph.D.
  • 年度 2005
  • 页码 215 p.
  • 总页数 215
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物医学工程;生物物理学;
  • 关键词

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