Frolova A Yu, Kutyakov S V, Martynov V I, Deyev S M, Pakhomov A A
M.M. Shemyakin and Yu.A. Ovchinnikov Institute of Bioorganic Chemistry of the Russian Academy of Sciences, Moscow, 117997 Russian Federation.
Acta Naturae. 2023 Oct-Dec;15(4):92-99. doi: 10.32607/actanaturae.26879.
In this work, we synthesized a green fluorescent dye derivative, 1,3,5,7-tetramethyl-BODIPY, with a heptyl substituent at the 8-position. The obtained highly hydrophobic compound was able to rapidly and irreversibly bind to eukaryotic cells. Incubation of cells with the dye over different periods of time or at different concentrations allowed us to control the degree of cell labeling and the level of fluorescence. This made it possible to modulate the fluorescence level of different eukaryotic cell cultures and then distinguish them by their level of fluorescence signal in the green channel in cytometric experiments. The labeled cells can be combined and further analyzed in the same test tube under identical conditions using the channels in which the dye does not fluoresce. This approach has been tested on a number of tumor cell cultures containing the HER2 receptor on their surface. The representation of the receptor in these cells was analyzed in one test tube in one run using a HER2-specific ligand based on the hybrid protein DARPin9_29-mCherry, which fluoresces in the red region of the spectrum.
在这项工作中,我们合成了一种绿色荧光染料衍生物,即8位带有庚基取代基的1,3,5,7-四甲基-BODIPY。所得到的高度疏水化合物能够快速且不可逆地与真核细胞结合。在不同时间段或不同浓度下用该染料孵育细胞,使我们能够控制细胞标记程度和荧光水平。这使得调节不同真核细胞培养物的荧光水平并在细胞计数实验中通过绿色通道中的荧光信号水平区分它们成为可能。标记的细胞可以合并,并在相同条件下于同一试管中使用染料不发荧光的通道进行进一步分析。这种方法已在多种表面含有HER2受体的肿瘤细胞培养物上进行了测试。使用基于杂交蛋白DARPin9_29-mCherry(在光谱的红色区域发荧光)的HER2特异性配体,在一个试管中一次运行就分析了这些细胞中受体的表达情况。