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Multiplexed cell for high-throughput FT-ICR MS

Multiplexed cell for high-throughput FT-ICR MS
用于高通量 FT-ICR MS 的多重池
批准号:
7404788
负责人:
Alexander Misharin
金额:
$10.0万
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-07-01 至 2009-12-31

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中文摘要
翻译
描述(由申请人提供):本提案的目的是开发一种利用傅里叶变换离子回旋共振(FT-ICR)质谱法对生物分子进行高通量质量分析的新技术。FT-ICR质谱仪在所有类型的质谱仪中提供最高的质量精度和分辨率,但分析速度是它们的缺点。所提议的技术解决了这个问题。它的主要特点是一种新的FT-ICR分析单元,它的设计和工作原理不同于任何其他的分析单元。在新细胞中,离子回旋运动的激发功能和离子回旋运动的检测功能在不同的隔间中分离。此外,检测发生在由同轴检测电极组成的隔室中。这种设计允许在回旋加速器频率的倍数上进行检测,从而提高了分析速度,而与传统的多电极电池相比,没有灵敏度损失和其他有害影响。分析的速度进一步提高,有一个室激发离子回旋运动和几个室同时检测不同离子群的回旋运动。该技术可使FT-ICR的分析速度提高一个数量级。
英文摘要
DESCRIPTION (provided by applicant): The purpose of this proposal is to develop a novel technology for high throughput mass analysis of biomolecules by Fourier transform ion cyclotron resonance (FT-ICR) mass spectrometry. FT-ICR mass spectrometers offer the highest mass accuracy and resolution among all types of mass analyzers, but speed of the analysis is their drawback. The proposed technology addresses this issue. The main its feature is a new FT-ICR analyzer cell which differs from any other analyzer cell in its design and operation principles. In the new cell, functions of the excitation of the ion cyclotron motion and its detection are separated between different compartments. Further, detection takes place in the compartment composed of coaxial detecting electrodes. Such design allows performing detection on a multiple of the cyclotron frequency, thus increasing the speed of the analysis, without loss of sensitivity and other detrimental effects as opposed to conventional multi-electrode cells. The speed of analysis is further increased by having one compartment for excitation of the ion cyclotron motion and several compartments for the simultaneous detection of the cyclotron motion of different ion populations. This technology can result in up to an order of the magnitude increase of the analysis speed in FT-ICR.
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会议论文
Monocyte-derived alveolar macrophage drives inflammatory response to lung ozone exposure
  • 批准号:
    10689120
  • 项目类别:
  • 资助金额:
    $60.88万
  • 财政年份:
    2022
  • 负责人:
    Alexander Misharin
  • 依托单位:
The Cell Phenotyping and Mouse Core
The Cell Phenotyping and Mouse Core
Lung transplant injury drives chronic lung allograft dysfunction via recruitment ofmonocyte-derived alveolar macrophages
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