Cho Heewon, Hong Na-Kyeong, Chang Young-Tae
Department of Chemistry, Pohang University of Science and Technology (POSTECH), Pohang 37673, Gyeongsangbuk-do, Republic of Korea.
Pharmaceutics. 2024 Mar 19;16(3):424. doi: 10.3390/pharmaceutics16030424.
Fluorescent bioprobes are invaluable tools for visualizing live cells and deciphering complex biological processes by targeting intracellular biomarkers without disrupting cellular functions. In addition to protein-binding concepts, fluorescent probes utilize various mechanisms, including membrane, metabolism, and gating-oriented strategies. This study introduces a novel fluorescent mechanism distinct from existing ways. Here, we developed a B cell selective probe, CDrB, with unique transport mechanisms. Through SLC-CRISPRa screening, we identified two transporters, SLCO1B3 and SLC25A41, by sorting out populations exhibiting higher and lower fluorescence intensities, respectively, demonstrating contrasting activities. We confirmed that SLCO1B3, with comparable expression levels in T and B cells, facilitates the transport of CDrB into cells, while SLC25A41, overexpressed in T lymphocytes, actively exports CDrB. This observation suggests that SLC25A41 plays a crucial role in discriminating between T and B lymphocytes. Furthermore, it reveals the potential for the reversible localization of SLC25A41 to demonstrate its distinct activity. This study is the first report to unveil a novel strategy of SLC by exporting the probe. We anticipate that this research will open up new avenues for developing fluorescent probes.
荧光生物探针是可视化活细胞和通过靶向细胞内生物标志物而不破坏细胞功能来解读复杂生物过程的宝贵工具。除了蛋白质结合概念外,荧光探针还利用各种机制,包括基于膜、代谢和门控的策略。本研究介绍了一种不同于现有方式的新型荧光机制。在此,我们开发了一种具有独特转运机制的B细胞选择性探针CDrB。通过SLC-CRISPRa筛选,我们分别通过对荧光强度较高和较低的群体进行分选,鉴定出两种转运蛋白SLCO1B3和SLC25A41,它们表现出相反的活性。我们证实,在T细胞和B细胞中表达水平相当的SLCO1B3促进CDrB转运进入细胞,而在T淋巴细胞中过表达的SLC25A41则积极输出CDrB。这一观察结果表明,SLC25A41在区分T淋巴细胞和B淋巴细胞中起关键作用。此外,它揭示了SLC25A41可逆定位以展示其独特活性的潜力。本研究是首次报道通过输出探针揭示SLC新策略的报告。我们预计这项研究将为开发荧光探针开辟新途径。