Department of Chemistry, Pohang University of Science and Technology (POSTECH), 37673, Pohang, Gyeongbuk, Republic of Korea.
Division of Oncology, Department of Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA.
Chem Asian J. 2022 Jun 15;17(12):e202200229. doi: 10.1002/asia.202200229. Epub 2022 May 2.
Cell labelling using a small fluorescent probe is an important technique in biomedical sciences. We previously developed a biocompatible and membrane-permeable probe, CO-1, which has low nonspecific binding affinity towards nontarget molecules. Although this background-free tame probe has been utilized for labelling of various intracellular biomolecules in live cells, the probes' backgroung-free staining mechanism was not fully understood. Here, we propose that Gating-Oriented Live-cell Distinction (GOLD) mechanism occurs when ABCB1 transporter removes unbound CO-1 molecules from mammalian cells and, in a minor role, DIRC2 pumps CO-1 out from lysosomes. We also showed that solute carrier transporters were not involved in carrying CO-1 inside of cells. The role of reporters in assisting the probes' influx-efflux was analyzed by the combination of CRISPR library sceenings and inhibitors test. In summary, tame probe CO-1 cellular staining occurs in a dual mechanism where the probe moves freely through the cells membrane, but its washable property can be directly related to the action of ABCB1 transporter.
使用小荧光探针进行细胞标记是生物医学科学中的一项重要技术。我们之前开发了一种生物相容性和膜通透性探针 CO-1,它对非靶标分子具有低的非特异性结合亲和力。尽管这种无背景的温和探针已被用于活细胞中各种细胞内生物分子的标记,但探针的无背景染色机制尚未完全理解。在这里,我们提出当 ABCB1 转运蛋白从哺乳动物细胞中去除未结合的 CO-1 分子时,会发生门控导向活细胞区分(GOLD)机制,而 DIRC2 泵以较小的作用将 CO-1 从溶酶体中泵出。我们还表明,溶质载体转运蛋白不参与将 CO-1 带入细胞内。通过 CRISPR 文库筛选和抑制剂测试的组合,分析了报告基因在协助探针内流-外流中的作用。总之,温和探针 CO-1 的细胞染色发生在一种双重机制中,探针可以自由穿过细胞膜,但它的可清洗性质可以直接与 ABCB1 转运蛋白的作用相关。