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UV resonance raman study of solution environment effect on poly-L-lysine conformation and resolution enhancement mechanism of two dimensional correlation spectroscopy.

机译:溶液环境对聚-L-赖氨酸构象的影响的紫外共振拉曼研究和二维相关光谱的分辨率增强机制。

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摘要

How proteins fold into compact, highly ordered and functional three-dimensional structures continues to challenge the modern science. UV resonance Raman (UVRR) is one of the advanced technologies used to study protein folding problem. In this thesis, by using UVRR spectroscopy, we examined solution environment effect on poly-L-lysine (PLL) conformation in great detail.;We investigated the sidechain electrostatic control of PLL conformation by examining the PLL conformational dependence on pH, the presence of NaCl and NaClO4, and temperature. At pH value below 7, PLL adopts the extended polyproline II (PPII) and 2.51-helix conformations. Increasing pH and the addition of NaClO4 induces PLL to form a high content of a-helix-like conformations (alpha-helix, pi-bulge/helix and turn structures) by decreasing the sidechain electrostatic repulsion. In contrast to NaClO4, we found that high concentrations of NaCl has negligible impact on the PLL conformation at low pH. Utilizing UVRR, we also quantitatively tracked temperature and NaClO4 concentration induced conformation changes of PLL. We experimentally determined the conformational population distributions and the energy landscape of PLL along the Ramachandran Psi angle under different solution conditions.;We measured the NaClO4 concentration dependence of PLL amide hydrogen exchange kinetics at pH 2.8 using UVRR spectroscopy. We found NaClO 4 slows the hydrogen exchange rates for the extended conformations and conformational exchange rates between the extended and alpha-helix-like conformations. We proposed a NaClO4 protection mechanism.;This thesis also includes the study of the resolution enhancement mechanism of generalized two-dimensional correlation spectroscopy (2D COS). Despite extensive study, the origin of the 2D COS spectral patterns for overlapping bands and the resolution enhancement mechanisms are not completely understood. By using the simulation method, we elucidated the origin of 2D COS spectral features and identified the conditions to resolve overlapping bands.
机译:蛋白质如何折叠成紧凑,高度有序和功能性的三维结构,继续挑战着现代科学。 UV共振拉曼(UVRR)是用于研究蛋白质折叠问题的先进技术之一。在本文中,我们使用UVRR光谱技术,详细研究了溶液环境对聚L-赖氨酸(PLL)构象的影响。 NaCl和NaClO4,以及温度。在低于7的pH值时,PLL采用扩展的聚脯氨酸II(PPII)和2.51螺旋构象。通过降低侧链静电排斥力,增加pH值和添加NaClO4可以诱导PLL形成高含量的a-螺旋状构象(α-螺旋,pi凸出/螺旋和转向结构)。与NaClO4相比,我们发现高浓度的NaCl在低pH值下对PLL构象的影响可忽略不计。利用UVRR,我们还定量跟踪了温度和NaClO4浓度引起的PLL构象变化。我们通过实验确定了不同溶液条件下沿Ramachandran Psi角的PLL的构象种群分布和能量分布。;我们使用UVRR光谱法测量了pH 2.8时PLL酰胺氢交换动力学的NaClO4浓度依赖性。我们发现NaClO 4减慢了扩展构象的氢交换速率以及扩展构象和α-螺旋样构象之间的构象交换率。我们提出了NaClO4的保护机理。本文还包括对广义二维相关光谱(2D COS)分辨率提高机理的研究。尽管进行了广泛的研究,但对于重叠频带的2D COS光谱图的起源和分辨率增强机制尚未完全了解。通过使用仿真方法,我们阐明了二维COS光谱特征的起源,并确定了解决重叠谱带的条件。

著录项

  • 作者

    Ma, Lu.;

  • 作者单位

    University of Pittsburgh.;

  • 授予单位 University of Pittsburgh.;
  • 学科 Chemistry Analytical.;Chemistry Biochemistry.;Biophysics General.
  • 学位 Ph.D.
  • 年度 2011
  • 页码 190 p.
  • 总页数 190
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-17 11:45:24

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