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Mass Analyzers: Common Types01:19

Mass Analyzers: Common Types

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The quadrupole mass analyzer consists of four cylindrical metal rods arranged in a diamond carrying a DC voltage and a radio-frequency AC voltage. The motion of ions through the quadrupole depends on the field strength, causing only ions of a certain m/z to resonate successfully and strike the detector at a given field strength. Though the transmission rate for these analyzers is high, the exact elemental composition of the sample is not determined because of low resolution; however, they are...
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Tandem Mass Spectrometry01:21

Tandem Mass Spectrometry

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Tandem mass spectrometry is a technique that uses multiple mass analyzers in series to obtain a higher selectivity and signal-to-noise ratio for the analyte. Instruments with multiple analyzers separated by an interaction cell enable secondary fragmentation and selected study of the fragment ions.
Secondary fragmentations occur in the interaction cell and can be induced by various factors. Fragmentation induced by collision with inert gases, such as N2, Ar, He, etc., is called collision-induced...
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UV–Vis Spectrometers01:14

UV–Vis Spectrometers

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The absorbance of UV and visible (UV–visible) radiations is measured using a UV–visible spectrophotometer. Deuterium lamps, which emit UV radiation, and tungsten lamps, which produce radiation in the visible region, are used as light sources in UV–visible spectrophotometers. A monochromator or prism is used for diffraction grating, i.e., to split the incoming radiation into different wavelengths. A system of slits is used to focus the desired wavelength on the sample cell.
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High-Resolution Mass Spectrometry (HRMS)01:15

High-Resolution Mass Spectrometry (HRMS)

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The resolution of a mass spectrometer depends on the efficiency of separating ions with different ion masses. The mass of an atom is approximated to the sum of the masses of protons and neutrons inside, considering the masses of protons and neutrons as equal. However, the masses of the proton (1.6726 × 10−24 g) and neutron (1.6749 × 10−24 g) are not truly equal. There is a minor error in the expression of atomic masses relative to the simplest atom of hydrogen. For...
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Mass Spectrometry: Complex Analysis01:21

Mass Spectrometry: Complex Analysis

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Mass spectrometry is an important technique for the identification of pure compounds. However, it has some limitations for the analysis of complex mixtures, often due to excessive fragmentation making the spectrum too complicated to decipher. Mass spectrometry can be combined with suitable separation methods in sequence, forming hyphenated methods, which are useful in the analysis of complex mixtures.
GC–MS is a powerful hyphenated method commonly used in forensics and environmental...
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Mass Spectrometers01:16

Mass Spectrometers

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This lesson details the instrumentation of a mass spectrometer—a physical instrument to perform mass spectrometry on analyte molecules and record the characteristic mass spectra. This is achieved via three chief functions:
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Molecular Beam Mass Spectrometry With Tunable Vacuum Ultraviolet VUV Synchrotron Radiation
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提升蛋白质分析:一种低压漂流管轨道轨道质谱仪,用于基于紫外线光解离的结构特征.

Jamie P Butalewicz1, James D Sanders1, Kyle J Juetten1

  • 1Department of Chemistry, The University of Texas at Austin, Austin, Texas 78712, United States.

Analytical chemistry
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紫外光解离质谱与离子流动性相结合,为蛋白质提供了结构选择性的结构信息. 该技术分析碎片离子到达时间,以揭示气相中的蛋白质折叠和延长.

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科学领域:

  • 蛋白质组学是指蛋白质组学.
  • 结构生物学 结构生物学
  • 分析化学 分析化学

背景情况:

  • 紫外光解离 (UVPD) 质谱 (MS) 是蛋白质结构特征的强大工具.
  • 解释UVPD碎片化模式,可以了解蛋白质的二级和三级结构.
  • 蛋白质的复杂性和形状的多样性在结构分析中提出了挑战.

研究的目的:

  • 将UVPD-MS与漂流管离子流动性相结合,用于对MS/MS进行形状选择性分析.
  • 开发一种方法来使用质谱测量解决蛋白质变异体.
  • 为了提高对气相蛋白质结构的理解.

主要方法:

  • 集成UVPD-MS与一个低压漂流管 (LPDT) 轨道飞船质谱仪.
  • 使用193nm的UVPD进行离子激活和碎片化.
  • 对碎片离子的到达时间分布 (ATD) 的分析,以表征符合性离子.

主要成果:

  • 集成的平台可以通过碎片离子ATD分析蛋白质对应物.
  • 通过对不同裂变点或电荷状态的ATD进行比较,可以了解蛋白质折叠.
  • 证明了获得形状选择性MS/MS数据的潜力.

结论:

  • 联合UVPD-MS和离子移动技术为气相蛋白质结构分析提供了一种新的方法.
  • 这种方法可以研究蛋白质折叠和延长.
  • 该平台推进了复杂蛋白质结构的表征.