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A New Dispersive Vibrational Circular Dichroism Instrument: Development, Testing, and Application.

机译:一种新型的分散振动圆二色性仪:开发,测试和应用。

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摘要

The primary goal of this thesis is to focus on the design and construction of a new dispersive vibrational circular dichrosim (VCD) instrument optimized for the measurement of mid-IR bands such as amide I and amide II vibrational modes of peptides and proteins (C=O stretching, and CN stretching-NH bending, respectively). VCD is a differential absorption (DeltaA = AL - AR) of left and right circularly polarized light by the excitation of molecular vibrational transitions in a chiral environment. The new VCD design was implemented to make a more compact VCD instrument for biological molecules, to increase signal to noise (S/N) ratio, to simultaneously collect the signals resulting from sample transmission and polarization modulation, and to digitally normalize these signals following a design of Diem.;In addition to describing the building of the new VCD instrument itself, we also collected spectra for peptides and proteins with different dominant secondary structures (alpha-helix, beta-sheet, and random coil), in order to compare the new dispersive VCD spectrometer to our previously constructed analogue-based dispersive VCD, and to some commercial Fourier Transform IR based VCD designs. In addition, we compared identical samples from old and new VCD instruments with comparable resolution and total measurement time. Our new compact dispersive VCD instrument exhibited improved S/N for the amide I` band region for biological molecules as compared to a previously built instrument in our laboratory.;Our first application studied 310-helical peptides with the new VCD spectrometer. The 310-helical synthesized peptides were studied in non-aqueous solvents, and we compare data gathered from the new VCD, IR, and Raman spectra of 310-helical synthesized peptides with two different amino-acid chain lengths. Simulations of the 310-helical peptide IR, Raman, and VCD provided a means of interpretation, since predictions of the conformational dependence of the relative separations of 13 C=O and 12C=O features and the exciton splitting of the 13C=O band in the doubly labeled species were in agreement with those seen experimentally.;A second application studied Amyloid fibrils, which are often associated with certain degenerative disorders. This study revealed a number of intriguing spectral properties using polyglutamic acid at low pH as a model system. Our results demonstrate how both IR absorption and enhanced VCD are measurable in such complex systems and provide spectra sensitive to subtle packing defects and the super helical structure of amyloid fibrils, thus shedding more light on the relationship between the fibrils' structure and their optical traits. We further detail ongoing or potential projects that would, moving forward, improve the performance of the VCD.
机译:本论文的主要目标是专注于新型分散振动圆二色谱(VCD)仪器的设计和构建,该仪器已优化用于测量中红外波段,如肽和蛋白质的酰胺I和酰胺II振动模式(C = O拉伸和CN拉伸-NH弯曲)。 VCD是通过手性环境中分子振动跃迁的激发来吸收左右圆偏振光的差分吸收(DeltaA = AL-AR)。实施新的VCD设计是为了制造一种用于生物分子的更紧凑的VCD仪器,以提高信噪比(S / N),同时收集由样品传输和偏振调制产生的信号,并对这些信号进行数字归一化处理。 Diem的设计;除了描述新的VCD仪器本身的构造之外,我们还收集了具有不同主要二级结构(α-螺旋,β-折叠和无规卷曲)的肽和蛋白质的光谱,以便比较新的色散VCD光谱仪,用于我们以前构建的基于模拟的色散VCD,以及一些基于商业傅里叶变换红外的VCD设计。此外,我们将来自新旧VCD仪器的相同样本在分辨率和总测量时间上进行了比较。与我们实验室中以前建造的仪器相比,我们的新型紧凑型分散式VCD仪器在生物分子的酰胺I'带区域具有更高的信噪比。我们的首次应用是使用新型VCD光谱仪研究了310螺旋肽。在非水溶剂中研究了310螺旋合成肽,我们比较了从具有两个不同氨基酸链长的310螺旋合成肽的新VCD,IR和拉曼光谱中收集的数据。 310螺旋肽IR,拉曼和VCD的仿真提供了一种解释的方法,因为预测了13 C = O和12C = O特征的相对间隔以及13C = O带的激子分裂的构象依赖性。双标记的物种与实验观察到的一致。第二个应用研究了淀粉样原纤维,其通常与某些变性疾病有关。这项研究揭示了使用低pH的聚谷氨酸作为模型系统的许多有趣的光谱特性。我们的结果表明,在这种复杂的系统中,IR吸收和VCD的增强是如何可测量的,并且提供了对细微堆积缺陷和淀粉样蛋白原纤维的超螺旋结构敏感的光谱,从而为原纤维结构与其光学特性之间的关系提供了更多的信息。我们将进一步详细介绍正在进行的或潜在的项目,这些项目将不断改善VCD的性能。

著录项

  • 作者

    Lakhani, Ahmed.;

  • 作者单位

    University of Illinois at Chicago.;

  • 授予单位 University of Illinois at Chicago.;
  • 学科 Chemistry Analytical.
  • 学位 Ph.D.
  • 年度 2011
  • 页码 206 p.
  • 总页数 206
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 遥感技术;
  • 关键词

  • 入库时间 2022-08-17 11:44:26

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