NESACBIO , University of Washington , Seattle , Washington 98195 , United States.
Department of Bioengineering , University of Washington , Seattle , Washington 98195 , United States.
Anal Chem. 2019 Dec 3;91(23):15073-15080. doi: 10.1021/acs.analchem.9b03763. Epub 2019 Nov 11.
Lipids have been recognized as key players in cell signaling and disease. Information on their location and distribution within a biological system, under varying conditions, is necessary to understand the contributions of different lipid species to an altered phenotype. Imaging mass spectrometry techniques, such as time-of-flight secondary ion mass spectrometry (ToF-SIMS) and matrix-assisted laser desorption/ionization (MALDI), are capable of revealing global lipid distributions in tissues in an untargeted fashion. However, to confidently identify the species present in a sample, orthogonal analyses like tandem MS (MS/MS) are often required. This can be accomplished by bulk sample analysis with liquid chromatography (LC)-MS/MS, which can provide confident lipid identifications, at the expense of losing location-specific information. Here, using planarian flatworms as a model system, we demonstrate that imaging gas cluster ion beam (GCIB)-ToF-SIMS has the unique capability to simultaneously detect, identify, and image lipid species with subcellular resolution in tissue sections. The parallel detection of both, intact lipids and their respective fragments, allows for unique identification of some species without the need of performing an additional orthogonal MS/MS analysis. This was accomplished by correlating intact lipid and associated fragment SIMS images. The lipid assignments, respective fragment identities, and locations gathered from ToF-SIMS data were confirmed via LC-MS/MS on lipid extracts and ultrahigh mass resolution MALDI-MS imaging. Together, these data show that the semidestructive nature of ToF-SIMS can be utilized advantageously to enable both confident molecular annotations and to determine the locations of species within a biological sample.
脂质已被认为是细胞信号转导和疾病的关键因素。了解不同脂质物种对表型改变的贡献,需要了解它们在生物系统内的位置和分布信息,这些信息在不同条件下会有所变化。飞行时间二次离子质谱(ToF-SIMS)和基质辅助激光解吸/电离(MALDI)等成像质谱技术能够以非靶向的方式揭示组织中全局脂质分布。然而,为了能够自信地鉴定样品中存在的物种,通常需要进行串联质谱(MS/MS)等正交分析。这可以通过液相色谱(LC)-MS/MS 对大块样品进行分析来实现,它可以提供有信心的脂质鉴定,但代价是失去位置特异性信息。在这里,我们使用扁形虫作为模型系统,证明了成像气相簇离子束(GCIB)-ToF-SIMS 具有独特的能力,可以在组织切片中以亚细胞分辨率同时检测、鉴定和成像脂质物种。完整脂质及其各自片段的平行检测允许对一些物种进行独特的鉴定,而无需进行额外的正交 MS/MS 分析。这是通过关联完整脂质和相关片段的 SIMS 图像来实现的。从 ToF-SIMS 数据中获得的脂质分配、各自片段的身份和位置,通过脂质提取物的 LC-MS/MS 和超高质量分辨率 MALDI-MS 成像得到了确认。总之,这些数据表明,ToF-SIMS 的半破坏性性质可以被有利地利用,以实现有信心的分子注释,并确定生物样品中物种的位置。