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Motor protein and microtubule mechanics: Application of a novel high-resolution optical trapping technique.

机译:运动蛋白和微管力学:一种新型的高分辨率光学捕获技术的应用。

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摘要

Using optical tweezers and a novel detection technique (a quadrant photodiode at the back focal plane or, BFP-QD), this thesis investigates two problems in biophysics, ncd motility and microtubule flexural rigidity. We use optically trapped microspheres to probe the samples. The technique detects the displacements of the microspheres relative to the trap center by monitoring the laser intensity shifts in the back focal plane of the microscope condenser. We use a quadrant diode to detect the shifts, which are due to far-field interference between the trapping laser and scattered laser light from the trapped object. The method yields high-resolution (nm-spatial and μsec-temporal), two-dimensional data, which is largely independent of trap position in the field of view.; We first studied the motility of ncd, a kinesin-related motor protein. Motor proteins are able to harness the energy of ATP hydrolysis to perform mechanical work for the cell. Many ncd molecules were adsorbed onto silica microspheres and their motions along the microtubule surface lattice were observed with the BFP-QD method. Since the method is two-dimensional, we were able to monitor axial and lateral motions simultaneously. The average axial velocity was 230 ± 30 nm/sec (average ± SD). The high temporal resolution allowed us to investigate dynamical parameters. Spectral analysis showed an increase in viscous drag near the surface for ncd-driven microspheres. In addition, we found that the binding of the motors to microtubules in the presence of the nonhydrolyzable nucleotide adenylylimidodiphosphate caused an increase in the motor elastic constraint.; Using a dual optical trap configuration in conjunction with the BFP-QD, we also investigated the elastic properties of taxol-stabilized microtubules. Cytoskeletal filaments are responsible for myriad structural cell functions. Our results were not readily interpreted by a standard bent strut treatment because of the finite size of the microspheres used as probes. I calculated an extension to the regular theory, which proved promising. The flexural rigidity was 3.2 ± 1.0 pNμm2 which is consistent with other results in the literature.
机译:本文使用光镊和一种新颖的检测技术(后焦平面处的象限光电二极管或BFP-QD),研究了生物物理学中的两个问题,即ncd运动性和微管弯曲刚度。我们使用光学捕获的微球来探测样品。该技术通过监视显微镜聚光镜的后焦平面中的激光强度偏移,来检测微球相对于阱中心的位移。我们使用一个象限二极管来检测偏移,这是由于捕获激光器和来自被捕获对象的散射激光之间的远场干扰引起的。该方法产生高分辨率(纳米空间和μsec时间)二维数据,这在很大程度上与陷阱的位置无关。我们首先研究了与驱动蛋白有关的运动蛋白ncd的运动能力。运动蛋白能够利用ATP水解的能量来执行细胞的机械工作。许多ncd分子被吸附到二氧化硅微球上,并通过BFP-QD方法观察到它们沿微管表面晶格的运动。由于该方法是二维的,因此我们能够同时监视轴向和横向运动。平均轴向速度为230±30nm / sec(平均±SD)。高时间分辨率使我们能够研究动力学参数。光谱分析显示,ncd驱动的微球在表面附近的粘性阻力增加。另外,我们发现在不可水解核苷酸腺苷酸二磷酸酯存在下,马达与微管的结合引起马达弹性约束的增加。使用双光阱配置结合BFP-QD,我们还研究了紫杉醇稳定的微管的弹性。细胞骨架丝负责无数结构细胞功能。由于用作探针的微球的尺寸有限,我们的结果无法通过标准的弯曲支撑杆处理轻松解释。我计算了常规理论的扩展,事实证明该方法很有希望。弯曲刚度为3.2±1.0pNμm 2 ,与文献中的其他结果一致。

著录项

  • 作者

    Allersma, Miriam W.;

  • 作者单位

    University of Michigan.;

  • 授予单位 University of Michigan.;
  • 学科 Biophysics General.; Physics Optics.
  • 学位 Ph.D.
  • 年度 2000
  • 页码 130 p.
  • 总页数 130
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物物理学;光学;
  • 关键词

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