Kemivagen 10, Gothenburg, Sweden.
Curr Opin Chem Biol. 2013 Oct;17(5):854-9. doi: 10.1016/j.cbpa.2013.07.017. Epub 2013 Aug 12.
Single-cell imaging mass spectrometry (IMS) is a powerful technique used to map the distributions of endogenous biomolecules with subcellular resolution. Currently, secondary ion mass spectrometry is the predominant technique for single-cell IMS, thanks to its submicron lateral resolution and surface sensitivity. However, recent methodological and technological developments aimed at improving the spatial resolution of matrix assisted laser desorption ionization (MALDI) have made this technique a potential platform of single-cell IMS. MALDI opens the field of single-cell IMS to new possibilities, including single cell proteomic imaging and atmospheric pressure analyses; however, sensitivity is a challenge. In this report, we estimate the availability of proteins and lipids in a single cell and discuss strategies employed to improve sensitivity at the single-cell level.
单细胞成像质谱(IMS)是一种强大的技术,用于以亚细胞分辨率绘制内源性生物分子的分布。目前,由于具有亚微米级的横向分辨率和表面灵敏度,二次离子质谱是单细胞 IMS 的主要技术。然而,最近旨在提高基质辅助激光解吸电离(MALDI)空间分辨率的方法和技术的发展,使得该技术成为单细胞 IMS 的潜在平台。MALDI 为单细胞 IMS 开辟了新的可能性,包括单细胞蛋白质组学成像和常压分析;然而,灵敏度是一个挑战。在本报告中,我们估计了单个细胞中蛋白质和脂质的可用性,并讨论了提高单细胞水平灵敏度所采用的策略。