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探索6-氮杂-2-硫代胸腺嘧啶作为基质辅助激光解吸/电离质谱成像(MALDI-MSI)基质用于福尔马林固定石蜡包埋临床样本的空间脂质组学研究

Exploring 6-aza-2-Thiothymine as a MALDI-MSI Matrix for Spatial Lipidomics of Formalin-Fixed Paraffin-Embedded Clinical Samples.

作者信息

Porto Natalia Shelly, Serrao Simone, Bindi Greta, Monza Nicole, Fumagalli Claudia, Denti Vanna, Piga Isabella, Smith Andrew

机构信息

Department of Medicine and Surgery, Proteomics and Metabolomics Unit, University of Milano-Bicocca, 20854 Vedano al Lambro, Italy.

Fondazione IRCCS San Gerardo dei Tintori, 20900 Monza, Italy.

出版信息

Metabolites. 2025 Aug 5;15(8):531. doi: 10.3390/metabo15080531.

DOI:10.3390/metabo15080531
PMID:40863150
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12388131/
Abstract

: In recent years, lipids have emerged as critical regulators of different disease processes, being involved in cancer pathogenesis, progression, and outcome. Matrix-Assisted Laser Desorption/Ionization Mass Spectrometry Imaging (MALDI-MSI) has significantly expanded the technology's reach, enabling spatially resolved profiling of lipids directly from tissue, including formalin-fixed paraffin-embedded (FFPE) specimens. In this context, MALDI matrix selection is crucial for lipid extraction and ionization, influencing key aspects such as molecular coverage and sensitivity, especially in such specimens with already depleted lipid content. Thus, in this work, we aim to explore the feasibility of mapping lipid species in FFPE clinical samples with MALDI-MSI using 6-aza-2-thiothymine (ATT) as a matrix of choice. : To do so, ATT performances were first compared to those two other matrices commonly used for lipidomic analyses, 2',5'-dihydroxybenzoic acid (DHB) and Norharmane (NOR), on lipid standards. : As a proof-of-concept, we then assessed ATT's performance for the MALDI-MSI analysis of lipids in FFPE brain sections, both in positive and negative ion modes, comparing results with those obtained from other commonly used dual-polarity matrices. In this context, ATT enabled the putative annotation of 98 lipids while maintaining a well-balanced detection of glycerophospholipids (60.2%) and sphingolipids (32.7%) in positive ion mode. It outperformed both DHB and NOR in the identification of glycolipids (3%) and fatty acids (4%). Additionally, ATT exceeded DHB in terms of total lipid count (62 vs. 21) and class diversity and demonstrated performance comparable to NOR in negative ion mode. Moreover, ATT was applied to a FFPE glioblastoma tissue microarray (TMA) evaluating the ability of this matrix to reveal biologically relevant lipid features capable of distinguishing normal brain tissue from glioblastoma regions. : Altogether, the results presented in this work suggest that ATT is a suitable matrix for pathology imaging applications, even at higher lateral resolutions of 20 μm, not only for proteomic but also for lipidomic analysis. This could enable the use of the same matrix type for the analysis of both lipids and peptides on the same tissue section, offering a unique strategic advantage for multi-omics studies, while also supporting acquisition in both positive and negative ionization modes.

摘要

近年来,脂质已成为不同疾病进程的关键调节因子,参与癌症的发病机制、进展及转归。基质辅助激光解吸/电离质谱成像(MALDI-MSI)显著拓展了该技术的应用范围,能够直接对包括福尔马林固定石蜡包埋(FFPE)标本在内的组织进行脂质的空间分辨分析。在此背景下,MALDI基质的选择对于脂质提取和电离至关重要,会影响分子覆盖范围和灵敏度等关键方面,尤其是在脂质含量已有所损耗的此类标本中。因此,在本研究中,我们旨在探索使用6-氮杂-2-硫代胸腺嘧啶(ATT)作为首选基质,通过MALDI-MSI对FFPE临床样本中的脂质种类进行成像的可行性。

为此,首先在脂质标准品上比较了ATT与另外两种常用于脂质组学分析的基质,即2',5'-二羟基苯甲酸(DHB)和去氢骆驼蓬碱(NOR)的性能。

作为概念验证,我们随后评估了ATT在正离子和负离子模式下对FFPE脑切片脂质进行MALDI-MSI分析的性能,并将结果与从其他常用的双极性基质获得的结果进行比较。在此背景下,ATT能够对98种脂质进行推定注释,同时在正离子模式下对甘油磷脂(60.2%)和鞘脂(32.7%)保持良好的平衡检测。在糖脂(3%)和脂肪酸(4%)的鉴定方面,它优于DHB和NOR。此外,在总脂质数量(62对21)和类别多样性方面,ATT超过了DHB,并且在负离子模式下表现出与NOR相当的性能。此外,ATT应用于FFPE胶质母细胞瘤组织微阵列(TMA),评估该基质揭示能够区分正常脑组织和胶质母细胞瘤区域的生物学相关脂质特征的能力。

总之,本研究结果表明,ATT是病理学成像应用的合适基质,即使在20μm的更高横向分辨率下,不仅适用于蛋白质组学分析,也适用于脂质组学分析。这使得能够在同一组织切片上使用相同类型的基质对脂质和肽进行分析,为多组学研究提供独特的战略优势,同时也支持在正离子和负离子电离模式下进行采集。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/908c/12388131/80feb8fcb08a/metabolites-15-00531-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/908c/12388131/7292ce89464e/metabolites-15-00531-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/908c/12388131/5b35a2570cff/metabolites-15-00531-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/908c/12388131/58f4913c0ceb/metabolites-15-00531-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/908c/12388131/80feb8fcb08a/metabolites-15-00531-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/908c/12388131/7292ce89464e/metabolites-15-00531-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/908c/12388131/5b35a2570cff/metabolites-15-00531-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/908c/12388131/58f4913c0ceb/metabolites-15-00531-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/908c/12388131/80feb8fcb08a/metabolites-15-00531-g004.jpg

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