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Bioothogonally applicable, pi-extended rhodamines for super-resolution microscopy imaging for intracellular proteins

机译:用于细胞内蛋白的超分辨率显微镜成像的生物速率适用,PI-扩展菱胺

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摘要

A set of new, bioorthogonally applicable tetrazine and polarity modulated double fluorogenic p-extended rhodamine probes were synthesized. Fluorogenicity and cell labeling experiments suggest that combination of the two quenching mechanisms allows low background labeling schemes even for probes with poor reactivity based fluorogenicity. Two of the new probes were tested in biological labeling schemes of intracellular proteins both in fixed and live cells. The labeled cells were subsequently subjected to confocal and STED imaging. These studies revealed that the rhodaindanes tested are membrane permeable, can stand the challenging environment of live cells and suitable for bioorthogonal, site-specific labeling of intracellular proteins. Furthermore, we found that both probes are suitable for subdiffraction imaging of the labeled structures using STED microscopy.
机译:合成了一组新的,生物健康适用的四嗪和极性调制的双荧光P延长罗丹明探针。 荧光性和细胞标记实验表明,即使基于反应性较差的荧光性,均匀的淬火机构的组合甚至允许低背景标记方案。 在固定和活细胞中的细胞内蛋白质的生物标记方案中测试了两种新探针。 随后将标记的细胞进行共焦和定量成像。 这些研究表明,测试的菱丹尼斯是膜可渗透的,可以忍受活细胞的挑战环境,适用于细胞内蛋白的生物正交,特异性标记。 此外,我们发现两个探针适用于使用STED显微镜的标记结构的分布成像。

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