Maastricht Multimodal Molecular Imaging (M4I) Institute, Division of Imaging Mass Spectrometry, Maastricht University , Maastricht, The Netherlands.
Advion , Harlow CM20 2NQ, United Kingdom.
Anal Chem. 2017 Oct 17;89(20):11143-11150. doi: 10.1021/acs.analchem.7b03512. Epub 2017 Oct 6.
Direct analysis by mass spectrometry (imaging) has become increasingly deployed in preclinical and clinical research due to its rapid and accurate readouts. However, when it comes to biomarker discovery or histopathological diagnostics, more sensitive and in-depth profiling from localized areas is required. We developed a comprehensive, fully automated online platform for high-resolution liquid extraction surface analysis (HR-LESA) followed by micro-liquid chromatography (LC) separation and a data-independent acquisition strategy for untargeted and low abundant analyte identification directly from tissue sections. Applied to tissue sections of rat pituitary, the platform demonstrated improved spatial resolution, allowing sample areas as small as 400 μm to be studied, a major advantage over conventional LESA. The platform integrates an online buffer exchange and washing step for removal of salts and other endogenous contamination that originates from local tissue extraction. Our carry over-free platform showed high reproducibility, with an interextraction variability below 30%. Another strength of the platform is the additional selectivity provided by a postsampling gas-phase ion mobility separation. This allowed distinguishing coeluted isobaric compounds without requiring additional separation time. Furthermore, we identified untargeted and low-abundance analytes, including neuropeptides deriving from the pro-opiomelanocortin precursor protein and localized a specific area of the pituitary gland (i.e., adenohypophysis) known to secrete neuropeptides and other small metabolites related to development, growth, and metabolism. This platform can thus be applied for the in-depth study of small samples of complex tissues with histologic features of ∼400 μm or more, including potential neuropeptide markers involved in many diseases such as neurodegenerative diseases, obesity, bulimia, and anorexia nervosa.
直接质谱分析(成像)由于其快速准确的读数,在临床前和临床研究中得到了越来越多的应用。然而,当涉及到生物标志物发现或组织病理学诊断时,需要从局部区域进行更敏感和深入的分析。我们开发了一种全面的、全自动的在线平台,用于高分辨率液体提取表面分析(HR-LESA),然后进行微液相色谱(LC)分离,并采用数据非依赖采集策略,直接从组织切片中对低丰度分析物进行非靶向和高通量鉴定。将该平台应用于大鼠垂体组织切片,结果表明其空间分辨率得到了提高,允许研究面积小至 400μm 的组织区域,这是对传统 LESA 的重大改进。该平台集成了在线缓冲交换和洗涤步骤,用于去除盐和其他源自局部组织提取的内源性污染物。我们的无交叉污染平台显示出良好的重现性,萃取间变异性低于 30%。该平台的另一个优势是通过采样后的气相离子迁移分离提供了额外的选择性。这使得能够区分共洗脱的等摩尔化合物,而无需额外的分离时间。此外,我们还鉴定了非靶向和低丰度分析物,包括来自前阿黑皮素原蛋白的神经肽,并定位了已知分泌神经肽和其他与发育、生长和代谢相关的小代谢物的垂体腺(即腺垂体)的特定区域。因此,该平台可用于对具有约 400μm 或更大组织学特征的复杂组织的小样本进行深入研究,包括参与许多疾病(如神经退行性疾病、肥胖症、贪食症和神经性厌食症)的潜在神经肽标志物。