Université de Lille 1, Inserm U-1192, Protéomique, Réponse Inflammatoire et Spectrométrie de Masse (PRISM), F-59000 Lille, France.
Université de Lille 1, Inserm U-1192, Laboratoire de Protéomique, Réponse Inflammatoire, Spectrométrie de Masse (PRISM), Department of Gynecology Oncology, Oscar Lambret Center, Lille, France.
Biochim Biophys Acta Proteins Proteom. 2017 Jul;1865(7):891-900. doi: 10.1016/j.bbapap.2016.11.002. Epub 2016 Nov 9.
Mass spectrometry (MS)-based microproteomics on localized regions of tissue sections was achieved by direct coupling of liquid microjunction microextraction with a nanoscale liquid chromatography-tandem MS, resulting in the identification of >500 protein groups from a region as small as 250μm in diameter representing only a few hundred of cells. The method was applied on the examination of benign and tumor regions initially defined by imaging mass spectrometry (IMS) analysis of a consecutive high grade serous ovarian tumor tissue section. Results identified the higher abundance of eukaryotic translation initiation factors eIF4A, its isoform eIF4A2, and eIF5A and its isoform eIF5A2, and lower abundance of actin-binding proteins OBSCN, TAGLN and CNN3 on tumor regions, concomitant with previous findings. This demonstrates the use of the method for downstream characterization of distinct regions identified by IMS. This article is part of a Special Issue entitled: MALDI Imaging, edited by Dr. Corinna Henkel and Prof. Peter Hoffmann.
基于质谱(MS)的组织切片局部区域的微蛋白质组学是通过液体微连接微萃取与纳升级液相色谱-串联质谱的直接耦合来实现的,结果从直径仅为 250μm 的小区域中鉴定出了>500 种蛋白质组,该区域仅代表几百个细胞。该方法应用于通过对连续高等级浆液性卵巢肿瘤组织切片的成像质谱(IMS)分析初步定义的良性和肿瘤区域进行检查。结果鉴定出肿瘤区域中真核翻译起始因子 eIF4A、其同工型 eIF4A2 和 eIF5A 及其同工型 eIF5A2 的丰度较高,而肌动蛋白结合蛋白 OBSCN、TAGLN 和 CNN3 的丰度较低,与之前的发现一致。这证明了该方法可用于对 IMS 鉴定的不同区域进行下游特征描述。本文是由 Corinna Henkel 博士和 Peter Hoffmann 教授编辑的题为“MALDI 成像”的特刊的一部分。