State Key Laboratory of Genetic Engineering, Human Phenome Institute, Department of Endocrinology and Metabolism, School of Life Sciences, Zhongshan Hospital, Fudan University, Shanghai 200438, China.
ImmuXell Biotech Ltd., Shanghai 201315, China.
Anal Chem. 2024 Oct 15;96(41):16236-16243. doi: 10.1021/acs.analchem.4c03075. Epub 2024 Sep 17.
The ability to dive deep into specific rare cell populations is critical for understanding tissue physiology and pathology across various biological domains. As single-cell RNA-seq flourishes, many newly discovered cell subtypes are defined by their transcriptomic markers. However, our ability to retrieve and analyze cells based on their nucleic acid markers remains underdeveloped. Here, we present Double Emulsion PCR-Initiated Cell sorting and Transcriptomic Sequencing (DEPICT-seq), a high-throughput droplet nucleic acid cytometry method that integrates batch cell fixation for cellular information preservation, double emulsion digital PCR-based cell sorting to target nucleic acid markers of interest, and in-depth full-length transcriptomic analyses at single-cell resolution. We utilize DEPICT-seq to isolate and characterize T cell receptor (TCR)-engineered T cells within a mixed population and also demonstrate a variation of the workflow by incorporating an RNase H-dependent PCR step to enrich full-length TCR sequences for paired single-cell TCR sequencing and transcriptomic profiling.
深入研究特定稀有细胞群体的能力对于理解各个生物学领域的组织生理学和病理学至关重要。随着单细胞 RNA 测序的蓬勃发展,许多新发现的细胞亚型是通过其转录组标志物定义的。然而,我们基于核酸标志物获取和分析细胞的能力仍不发达。在这里,我们提出了双乳液 PCR 引发的细胞分选和转录组测序(DEPICT-seq),这是一种高通量液滴核酸细胞计量法,它集成了批量细胞固定以保存细胞信息、基于双乳液数字 PCR 的细胞分选以靶向感兴趣的核酸标志物,以及单细胞分辨率的深度全长转录组分析。我们利用 DEPICT-seq 从混合群体中分离和表征 T 细胞受体 (TCR)-工程化 T 细胞,并通过引入依赖 RNase H 的 PCR 步骤来展示工作流程的变化,以富集全长 TCR 序列,用于配对的单细胞 TCR 测序和转录组分析。