Egbejiogu Blessing C, Donnarumma Fabrizio, Murray Kermit K
Department of Chemistry, Louisiana State University, Baton Rouge, Louisiana 70803, United States.
J Am Soc Mass Spectrom. 2024 Dec 4;35(12):2993-3001. doi: 10.1021/jasms.4c00299. Epub 2024 Nov 4.
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.
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普遍存在且极为宝贵的资源。然而,由于蛋白质交联和化学修饰,FFPE组织蛋白质组学颇具挑战性。激光烧蚀采样能够在高空间控制和可重复性的条件下,从组织切片中精确去除材料,用于液相色谱-串联质谱联用的离线蛋白质组学分析。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采样,以便后续对蛋白质进行鉴定和定量。结果发现,与新鲜冷冻(FF)组织激光烧蚀采样相比,FFPE组织激光烧蚀采样鉴定出的蛋白质更多,并且激光烧蚀比手动解剖FFPE组织鉴定出的蛋白质更多。与先前的研究不同,未观察到由于残留交联导致亲水性蛋白质的损失。激光烧蚀微采样对蛋白质的有效捕获归因于组织的有效激光破碎,这有利于蛋白质的下游处理。