Infrared Laser Ablation and Capture of Formalin-Fixed Paraffin-Embedded Tissue.

IF 3.1 2区 化学 Q2 BIOCHEMICAL RESEARCH METHODS Journal of the American Society for Mass Spectrometry Pub Date : 2024-11-04 DOI:10.1021/jasms.4c00299
Blessing C Egbejiogu, Fabrizio Donnarumma, Kermit K Murray
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Abstract

Formalin-fixed paraffin-embedded (FFPE) tissue is a ubiquitous and invaluable resource for biomedical research and clinical applications. However, FFPE tissue proteomics is challenging due to protein cross-linking and chemical modification. Laser ablation sampling allows precise removal of material from tissue sections with high spatial control and reproducibility for offline proteomics by liquid chromatography coupled with tandem mass spectrometry. In this work, we used a pulsed mid-infrared laser for microsampling of rat liver tissue for subsequent identification and quantification of proteins. It was found that more proteins were identified by FFPE tissue laser ablation sampling compared to fresh frozen (FF) tissue laser ablation sampling and that more proteins were identified by laser ablation than by manual dissection of FFPE tissue. In contrast to previous studies, no loss of hydrophilic proteins due to residual cross-linking was observed. The efficient capture of proteins by laser ablation microsampling is attributed to efficient laser breakup of the tissue which facilitates downstream processing of the proteins.

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红外线激光烧蚀和捕获福尔马林固定的石蜡包埋组织。
福尔马林固定石蜡包埋(FFPE)组织是生物医学研究和临床应用中无处不在的宝贵资源。然而,由于蛋白质的交联和化学修饰,FFPE 组织蛋白质组学具有挑战性。激光烧蚀取样可精确去除组织切片上的物质,具有高度的空间控制性和可重复性,可用于液相色谱-串联质谱离线蛋白质组学研究。在这项工作中,我们使用脉冲中红外激光对大鼠肝脏组织进行微取样,随后对蛋白质进行鉴定和定量。研究发现,与新鲜冷冻(FF)组织激光消融取样相比,FFPE组织激光消融取样能鉴定出更多的蛋白质,而且与人工解剖FFPE组织相比,激光消融取样能鉴定出更多的蛋白质。与之前的研究不同的是,没有观察到亲水性蛋白质因交联残留而损失。激光烧蚀显微取样技术之所以能有效捕获蛋白质,是因为激光能有效分解组织,从而促进蛋白质的下游处理。
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来源期刊
CiteScore
5.50
自引率
9.40%
发文量
257
审稿时长
1 months
期刊介绍: The Journal of the American Society for Mass Spectrometry presents research papers covering all aspects of mass spectrometry, incorporating coverage of fields of scientific inquiry in which mass spectrometry can play a role. Comprehensive in scope, the journal publishes papers on both fundamentals and applications of mass spectrometry. Fundamental subjects include instrumentation principles, design, and demonstration, structures and chemical properties of gas-phase ions, studies of thermodynamic properties, ion spectroscopy, chemical kinetics, mechanisms of ionization, theories of ion fragmentation, cluster ions, and potential energy surfaces. In addition to full papers, the journal offers Communications, Application Notes, and Accounts and Perspectives
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Infrared Laser Ablation and Capture of Formalin-Fixed Paraffin-Embedded Tissue. Quantitative Analysis of Drugs in a Mimetic Tissue Model Using Nano-DESI on a Triple Quadrupole Mass Spectrometer. Development of a Novel Label-Free Subunit HILIC-MS Method for Domain-Specific Free Thiol Identification and Quantitation in Therapeutic Monoclonal Antibodies. Single Cell MALDI-MSI Analysis of Lipids and Proteins within a Replicative Senescence Fibroblast Model. Processing Next-Generation Mass Spectrometry Imaging Data: Principal Component Analysis at Scale.
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