Wellman Center for Photomedicine, Harvard Medical School, Massachusetts General Hospital, 65 Landsdowne St. UP-5, Cambridge, Massachusetts 02139, USA.
Lab Chip. 2017 Aug 8;17(16):2777-2784. doi: 10.1039/c7lc00220c.
The ability to label individual cells is useful for single-cell-level studies of complex cellular interactions and heterogeneity. Optically readable cell labeling is attractive as it can be investigated non-invasively and repeatedly at high speeds. Here, we demonstrate the feasibility of large-scale cell barcoding and identification using fluorescent polystyrene microbeads loaded into cells. Intracellular beads with different diameters in a range of 5 to 12 μm generate spectrally distinguished features or barcodes. A microfluidic chip was used to measure fluorescence resonance peaks emitted from individual cells. An algorithm comparing the peak wavelengths to a reference barcode library allowed barcode identification with high accuracy. This work provides a guideline to increase the number of unique identifiers and reduce various false-positive and false-negative errors.
对单个细胞进行标记的能力对于复杂细胞相互作用和异质性的单细胞水平研究非常有用。光学可读的细胞标记具有吸引力,因为它可以在高速下进行非侵入性和重复的研究。在这里,我们展示了使用加载到细胞中的荧光聚苯乙烯微球进行大规模细胞编码和识别的可行性。在 5 到 12 μm 的范围内具有不同直径的细胞内珠子产生光谱上可区分的特征或条形码。使用微流控芯片测量从单个细胞发射的荧光共振峰。一种将峰值波长与参考条形码库进行比较的算法允许以高精度识别条形码。这项工作为增加唯一标识符的数量和减少各种假阳性和假阴性错误提供了指导。