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首页> 外文期刊>Journal of the American Society for Mass Spectrometry >Generation and detection of multiply-charged peptides and proteins by matrix-assisted laser desorption electrospray ionization (MALDESI) Fourier transform ion cyclotron resonance mass spectrometry
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Generation and detection of multiply-charged peptides and proteins by matrix-assisted laser desorption electrospray ionization (MALDESI) Fourier transform ion cyclotron resonance mass spectrometry

机译:基质辅助激光解吸电喷雾电离(MALDESI)傅里叶变换离子回旋共振质谱法生成和检测多电荷肽和蛋白质

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摘要

We report the coupling of a hybrid ionization source, matrix-assisted laser desorption electrospray ionization (MALDESI), to a Fourier transform-ion cyclotron resonance mass spectrometer (FT-ICR MS). The details of the source design and initial data are presented. Analysis of peptides and proteins ranging from 1 to 8.6 kDa resulted in high resolving power single-acquisition FT-ICR mass spectra with average charge-states highly correlated to those obtained by nanoESI, thus, providing strong evidence that the ESI process dictates the observed charge-state distribution. Importantly, unlike the recently introduced electrospray assisted laser desorption ionization (ELDI) source reported by Shiea and coworkers [1, 2], the data we have obtained to date rely on the use of an organic acid matrix. The results presented herein provide insight into the charging mechanism of this emerging ionization approach, while also expanding the utility of FT-ICR MS for top-down protein and complex mixture analysis.
机译:我们报告耦合到傅立叶变换离子回旋共振质谱仪(FT-ICR MS)的混合电离源,基质辅助激光解吸电喷雾电离(MALDESI)。给出了源设计和初始数据的详细信息。对1至8.6 kDa范围内的肽和蛋白质进行分析可得到高分辨能力的单捕获FT-ICR质谱图,其平均电荷态与nanoESI获得的质谱高度相关,因此,有力证据表明ESI过程决定了所观察到的电荷状态分布。重要的是,与Shiea及其同事报道的最近引入的电喷雾辅助激光解吸电离(ELDI)源[1、2]不同,我们迄今为止获得的数据依赖于有机酸基质的使用。本文介绍的结果提供了对这种新兴电离方法的充电机制的洞察力,同时还扩展了FT-ICR MS用于自上而下的蛋白质和复杂混合物分析的实用性。

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