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首页> 外文期刊>Analytical chemistry >Design and Performance of a Novel Interface for Combined Matrix-Assisted Laser Desorption Ionization at Elevated Pressure and Electrospray Ionization with Orbitrap Mass Spectrometry
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Design and Performance of a Novel Interface for Combined Matrix-Assisted Laser Desorption Ionization at Elevated Pressure and Electrospray Ionization with Orbitrap Mass Spectrometry

机译:用横梁质谱法在升压和电喷雾电离下组合基质辅助激光解吸电离的新界面的设计和性能

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摘要

Matrix-Assisted Laser Desorption Ionization, MALDI, has been increasingly used in a variety of biomedical applications, including tissue imaging of clinical tissue samples, and in drug discovery and development. These studies strongly depend on the performance of the analytical instrumentation and would drastically benefit from improved sensitivity, reproducibility, and mass/spatial resolution. In this work, we report on a novel combined MALDI/ESI interface, which was coupled to different Orbitrap mass spectrometers (Elite and Q Exactive Plus) and extensively characterized with peptide and protein standards, and in tissue imaging experiments. In our approach, MALDI is performed in the elevated pressure regime (5-8 Torr) at a spatial resolution of 15-30 mu m, while ESI-generated ions are injected orthogonally to the interface axis. We have found that introduction of the MALDI-generated ions into an electrodynamic dual funnel interface results in increased sensitivity characterized by a limit of detection of,similar to 400 zmol, while providing a mass measurement accuracy of 1 ppm and a mass resolving power of 120 OW in analysis of protein digests. In tissue imaging experiments, the MALDI/ESI interface has been employed in experiments with rat brain sections and was shown to be capable of visualizing and spatially characterizing very low abundance analytes separated only by 20 mDa. Comparison of imaging data has revealed excellent agreement between the MALDI and histological images.
机译:MATRIX辅助激光解吸电离,MALDI越来越多地用于各种生物医学应用,包括临床组织样本的组织成像,以及药物发现和发育。这些研究强烈依赖于分析仪器的性能,从而大大享受改善的灵敏度,再现性和质量/空间分辨率。在这项工作中,我们报告了一种新颖的MALDI / ESI界面,其耦合到不同的侧面射体光谱仪(ELITE和Q.辐射加),并随着肽和蛋白质标准的广泛表征,以及组织成像实验。在我们的方法中,MALDI以15-30μm的空间分辨率在升压状态(5-8托)中进行,而ESI产生的离子在界面轴线上被正角地注射。我们发现将MALDI生成的离子引入电动双漏斗界面导致的灵敏度增加,其特征在于,类似于400 Zmol的检测限,同时提供1ppm的质量测量精度和120的质量分辨率蛋白质消化分析。在组织成像实验中,MALDI / ESI界面已在大鼠脑切片的实验中使用,并且被证明能够可视化和空间表征非常低的丰度分析仅在20MDA中分离。成像数据的比较显示了MALDI和组织学图像之间的良好协议。

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