Micro-Pillar Array Column Separations for Proteomics of Liver Organoids

A. Aizenshtadt, Lise Midtøy, B. Thiede, Stefan Krauss, H. Røberg-Larsen, S. Wilson
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Abstract

Organoids are laboratory-grown three-dimensional (3D) models of organs and are emerging tools for studies into developmental biology, drug discovery, and toxicology. Organoids are complex biological materials, and proteomics studies of organoids can benefit from applying high-resolution chromatography devices before mass spectrometric analysis. Micro-pillar array columns have been shown to provide excellent resolution of peptide products of proteolytic digestion of proteins for bottom-up proteomics.This article describes a workflow incorporating a micro-pillar array column for mapping the proteome of human stem cell-derived liver organoids (sample preparation using a SPEED protocol) using trapped ion mobility time-of-flight mass spectrometry (timsTOF-MS).
肝类器官蛋白质组学的微柱阵列柱分离
类器官是实验室培养的三维(3D)器官模型,是研究发育生物学、药物发现和毒理学的新兴工具。类器官是复杂的生物材料,在质谱分析之前应用高分辨率色谱设备可以使类器官的蛋白质组学研究受益。微柱阵列柱已被证明可以为自下而上的蛋白质组学提供蛋白质水解消化肽产物的极好分辨率。本文描述了一种工作流程,采用微柱阵列柱,利用捕获离子迁移率飞行时间质谱(timsTOF-MS)绘制人类干细胞衍生的肝类器官的蛋白质组图(样品制备使用SPEED协议)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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