Center for Self-assembly and Complexity, Institute for Basic Science (IBS), Pohang, 37673, Republic of Korea.
School of Interdisciplinary Bioscience and Bioengineering, Pohang University of Science and Technology (POSTECH), Pohang, 37673, Republic of Korea.
Angew Chem Int Ed Engl. 2022 Sep 5;61(36):e202202095. doi: 10.1002/anie.202202095. Epub 2022 Jul 28.
T and B lymphocytes are two major adaptive immune cells in the human defense system. To real-time monitor their diverse functions, a live-cell-selective probe for only one cell type is need to investigate the complex interaction of the immune cells. Herein, a small-molecule probe CDyB for live B cells is developed by an unbiased fluorescence library screening. The cell selectivity was confirmed by multiparametric single-cell analysis using CyTOF. Through a systematic SLC-CRISPRi library screening, the molecular target of CDyB was identified as SLC35C2 transporter based on a gating-oriented live-cell distinction (GOLD) mechanism. The gene expression analysis and knock-out experiments validated that the SLC35C2 transporter was the target for CDyB distinction. Interestingly, when CDyB was applied to study B cell development, the CDyB fluorescence and SLC35C2 expression were positively correlated with the B cell maturation process, and not involved in the T cell development.
T 和 B 淋巴细胞是人体防御系统中的两种主要适应性免疫细胞。为了实时监测它们的多种功能,需要有一种仅针对一种细胞类型的活细胞选择性探针来研究免疫细胞的复杂相互作用。在此,通过无偏荧光文库筛选开发了一种用于活 B 细胞的小分子探针 CDyB。使用 CyTOF 通过多参数单细胞分析确认了细胞选择性。通过系统的 SLC-CRISPRi 文库筛选,基于门控导向活细胞区分 (GOLD) 机制,确定 CDyB 的分子靶标为 SLC35C2 转运蛋白。基因表达分析和敲除实验验证了 SLC35C2 转运蛋白是 CDyB 区分的靶标。有趣的是,当 CDyB 被应用于研究 B 细胞发育时,CDyB 荧光和 SLC35C2 表达与 B 细胞成熟过程呈正相关,而不涉及 T 细胞发育。