Neupert Susanne, Rubakhin Stanislav S, Sweedler Jonathan V
Department of Chemistry and the Beckman Institute for Advanced Science and Technology, University of Illinois Urbana-Champaign, Urbana, IL 61801, USA.
Chem Biol. 2012 Aug 24;19(8):1010-9. doi: 10.1016/j.chembiol.2012.05.023.
Pinpointing a specific cell from within a relatively uniform cell population to determine its chemical content presents a challenging bioanalytical task. Immunocytochemistry is the classical method used to localize specific molecules and, hence, selected cells. Mass spectrometry also probes endogenous molecules such as neuropeptides within a cell. Here, these two approaches are hyphenated to allow microchemical analysis of immunocytochemical-selected peptidergic neurons. This two-step strategy utilizes antibody-based localization of cells containing selected biomarkers to isolate the cell(s) of interest, followed by peptidomic analysis via mass spectrometry. Applicable to a broad range of analyte and cell types, the strategy was used to successfully profile neuropeptides from individual immunostained insect neurons stored for up to 2 weeks as well as from tissues preserved for 42 weeks.
从相对均匀的细胞群体中精准找出特定细胞以确定其化学组成,是一项具有挑战性的生物分析任务。免疫细胞化学是用于定位特定分子从而确定所选细胞的经典方法。质谱分析也可探测细胞内的内源性分子,如神经肽。在此,将这两种方法联用,以便对免疫细胞化学选定的肽能神经元进行微化学分析。这种两步策略利用基于抗体的方法定位含有选定生物标志物的细胞,以分离出感兴趣的细胞,随后通过质谱进行肽组分析。该策略适用于广泛的分析物和细胞类型,已成功用于分析存储长达2周的单个免疫染色昆虫神经元以及保存42周的组织中的神经肽。