Bundesanstalt für Materialforschung und -prüfung (BAM) , Richard-Willstätter-Str. 11 , 12489 Berlin , Germany.
Department of Chemistry and SALSA , Humboldt Universität zu Berlin , Brook-Taylor-Str. 2 , 12489 Berlin , Germany.
Anal Chem. 2019 Sep 17;91(18):11520-11528. doi: 10.1021/acs.analchem.9b00198. Epub 2019 Aug 28.
Arraying of single cells for mass spectrometric analysis is a considerable bioanalytical challenge. In this study, we employ a novel single cell arraying technology for quantitative analysis and isotopic fingerprinting by laser ablation inductively coupled plasma time-of-flight mass spectrometry (LA-ICP-TOF-MS). The single cell arraying approach is based on a piezo-acoustic microarrayer with software for automated optical detection of cells within the piezo dispense capillary (PDC) prior to arraying. Using optimized parameters, single cell occupancy of >99%, high throughput (up to 550 cells per hour), and a high cell recovery of >66% is achieved. LA-ICP-TOF-MS is employed to detect naturally occurring isotopes in the whole mass range as fingerprints of individual cells. Moreover, precise quantitative determination of metal-containing cell dyes is possible down to contents of ∼100 ag using calibration standards which were produced using the same arrayer.
单细胞阵列用于质谱分析是一项具有挑战性的生物分析任务。在这项研究中,我们采用了一种新型的单细胞阵列技术,通过激光烧蚀电感耦合等离子体质谱(LA-ICP-TOF-MS)进行定量分析和同位素指纹分析。单细胞阵列方法基于带有软件的压电微阵列,用于在阵列之前自动光学检测 PD C 内的细胞。使用优化的参数,可以实现 >99%的单细胞占有率、高通量(高达 550 个细胞/小时)和 >66%的高细胞回收率。LA-ICP-TOF-MS 用于检测整个质量范围内的天然存在同位素作为单个细胞的指纹。此外,使用相同的阵列器制备的校准标准,可以对含量低至 ∼100 ag 的含金属细胞染料进行精确的定量测定。