化学
质谱成像
质谱法
等压线
三级四极质谱仪
解吸电喷雾电离
电喷雾电离
分析化学(期刊)
生物分子
选择性反应监测
电离
色谱法
化学电离
串联质谱法
离子
原子物理学
有机化学
生物化学
核子
物理
作者
Miranda R. Weigand,Daisy Unsihuay,Manxi Yang,Hang Hu,Emerson Hernly,Matthew Muhoberac,Shane E. Tichy,Julia Laskin
标识
DOI:10.1021/acs.analchem.3c04705
摘要
Mass spectrometry imaging (MSI) is widely used for examining the spatial distributions of molecules in biological samples. Conventional MSI approaches, in which molecules extracted from the sample are distinguished based on their mass-to-charge ratio, cannot distinguish between isomeric species and some closely spaced isobars. To facilitate isobar separation, MSI is typically performed using high-resolution mass spectrometers. Nevertheless, the complexity of the mixture of biomolecules observed in each pixel of the image presents a challenge, even for modern mass spectrometers with the highest resolving power. Herein, we implement nanospray desorption electrospray ionization (nano-DESI) MSI on a triple quadrupole (QqQ) mass spectrometer for the spatial mapping of isobaric and isomeric species in biological tissues. We use multiple reaction monitoring acquisition mode (MRM) with unit mass resolution to demonstrate the performance of this new platform by imaging lipids in mouse brain and rat kidney tissues. We demonstrate that imaging in MRM mode may be used to distinguish between isobaric phospholipids requiring a mass resolving power of 3,800,000. Additionally, we have been able to image eicosanoid isomers, a largely unexplored class of signaling molecules present in tissues at low concentrations, in rat kidney tissue. This new capability substantially enhances the specificity and selectivity of MSI, enabling spatial localization of species that remain unresolved in conventional MSI experiments.
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