首页> 外文期刊>Journal of the American Society for Mass Spectrometry >Twelve Million Resolving Power on 4.7 T Fourier Transform Ion Cyclotron Resonance Instrument with Dynamically Harmonized Cell-Observation of Fine Structure in Peptide Mass Spectra
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Twelve Million Resolving Power on 4.7 T Fourier Transform Ion Cyclotron Resonance Instrument with Dynamically Harmonized Cell-Observation of Fine Structure in Peptide Mass Spectra

机译:动态调谐细胞观察的4.7 T傅里叶变换离子回旋共振仪上的1200万分辨力在肽质谱图中

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摘要

Resolving power of about 12,000 000 at m/z 675 has been achieved on low field homogeneity 4.7 T magnet using a dynamically harmonized Fourier transform ion cyclotron resonance (FT ICR) cell. Mass spectra of the fine structure of the isotopic distribution of a peptide were obtained and strong discrimination of small intensity peaks was observed in case of resonance excitation of the ions of the whole isotopic cluster to the same cyclotron radius. The absence of some peaks from the mass spectra of the fine structure was explained basing on results of computer simulations showing strong ion cloud interactions, which cause the coalescence of peaks with m/z close to that of the highest magnitude peak. The way to prevent peak discrimination is to excite ion clouds of different m/z to different cyclotron radii, which was demonstrated and investigated both experimentally and by computer simulations.
机译:使用动态协调的傅立叶变换离子回旋共振(FT ICR)电池,在低磁场均匀性4.7 T磁体上已实现了m / z 675时约12,000 000的分辨能力。获得了肽同位素分布的精细结构的质谱图,并且在将整个同位素簇的离子共振激发到相同的回旋加速器半径的情况下,观察到了对小的强度峰的强分辨。基于计算机模拟的结果解释了精细结构的质谱图中不存在某些峰,该结果显示了强烈的离子云相互作用,这导致m / z接近最高峰的峰的合并。防止峰歧视的方法是将不同m / z的离子云激发到不同的回旋加速器半径,这已通过实验和计算机模拟进行了论证和研究。

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