AI Article Synopsis

  • Fluorescent bioprobes are essential for studying live cells and biological processes by targeting specific intracellular biomarkers without disrupting cell functions.
  • This study introduces a new fluorescent probe, CDrB, designed to selectively target B cells, utilizing unique transport mechanisms identified through SLC-CRISPRa screening.
  • The research highlights two transporters, SLCO1B3, which imports CDrB into both T and B cells, and SLC25A41, which exports CDrB and shows potential for distinguishing between T and B lymphocytes, paving the way for innovative fluorescent probe development.

Article Abstract

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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10974409PMC
http://dx.doi.org/10.3390/pharmaceutics16030424DOI Listing

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