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Solid-State NMR Derived Structure: Membrane-Bound Polypetides to Protein

Solid-State NMR Derived Structure: Membrane-Bound Polypetides to Protein
固态 NMR 衍生结构:膜结合的多肽与蛋白质
批准号:
9603935
负责人:
Timothy Cross
金额:
$36.0万
依托单位:
依托单位国家:
美国
项目类别:
Continuing Grant
财政年份:
1997
资助国家:
美国
项目状态:
已结题
起止时间:
1997-02-01 至 2000-04-30

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英文摘要
9603935 Cross The knowledge gained from the gramicidin studies will now be used to face the challenges associated with a biosynthetically prepared protein, M2 protein, studied as a dilute species in a lipid bilayer. Improvements in sensitivity will come from modications in the sample geometry, increased field strength and improvements in the experimental protocols. Linewidths in the M2 samples are primarily dominated by sample heterogeneity which through adjustments in sample preparation techniques can be addressed and there is also reasonable expectations that linewidths (in ppm) at least in some cases will decrease the increasing field strength. The mathematical challenges will involve the characterization of imperfect alpha-helices that are prevalent in membrane proteins. The work will take this solid state NMR method that utilizes orientational rather than distance constraints and apply it to a "real" protein system. High technology methods involving Nuclear Magnetic resonance (NMR) spectroscopy will be developed to solve the three-dimensional structures of macromolecules. Typically such structures are determined by diffraction methods applied to crystallized samples, but there are many important macromolecules that are not crystallizable. This unique NMR approach uses samples that are uniformly aligned, in other words they are oriented in one dimension, while crystals involve three-dimensional order. The molecular system that will be used for demonstrating these methods is protein that forms an ion channel in membranes. The NMR data obtained will be analyzed by new mathematical approaches that will be generally applicable to many molecular systems. Overall, the development of this structure determination approach will open new avenues of research for a great many types of molecules that are not easily crystallized. The work will provide great training opportunities for graduate students and postdocs in an interdisciplinary environment where molecular biology, synthetic chemistr y, NMR spectroscopy, NMR hardware development, molecular modeling and mathematical analysis occur in the confines of this research effort.
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Membrane Protein Solid State NMR: PISEMA Development and the M2 Tetramer Structure
  • 批准号:
    0235774
  • 项目类别:
    Continuing Grant
  • 资助金额:
    $51.63万
  • 财政年份:
    2003
  • 负责人:
    Timothy Cross
  • 依托单位:
Solid-State NMR Derived Structure: Backbone of Influenza A M2 Protein
  • 批准号:
    9986036
  • 项目类别:
    Continuing Grant
  • 资助金额:
    $40.5万
  • 财政年份:
    2000
  • 负责人:
    Timothy Cross
  • 依托单位:
Acquisition of 830 and 900 MHz NMR Consoles
  • 批准号:
    9725059
  • 项目类别:
    Standard Grant
  • 资助金额:
    $55.78万
  • 财政年份:
    1998
  • 负责人:
    Timothy Cross
  • 依托单位:
Ultra-High Resolution Structure and Dynamics of Bilayer Bound Polypeptides
  • 批准号:
    9317111
  • 项目类别:
    Continuing Grant
  • 资助金额:
    $34.5万
  • 财政年份:
    1994
  • 负责人:
    Timothy Cross
  • 依托单位:
国内基金
海外基金
Simulation and certification of the ground state of many-body systems on quantum simulators
  • 批准号:
    --
  • 项目类别:
    --
  • 资助金额:
    40万元
  • 批准年份:
    2020
  • 负责人:
    Abolfazl Bayat
  • 依托单位:
Cortical control of internal state in the insular cortex-claustrum region
微波有源Scattering dark state粒子的理论及应用研究
  • 批准号:
    61701437
  • 项目类别:
    青年科学基金项目
  • 资助金额:
    28.0万元
  • 批准年份:
    2017
  • 负责人:
    李欢
  • 依托单位: