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提高硅罗丹明的亮度和稳定性,用于活细胞中线粒体的超分辨成像。

Improving Brightness and Stability of Si-Rhodamine for Super-Resolution Imaging of Mitochondria in Living Cells.

机构信息

Key Laboratory of Medicinal Chemistry and Molecular Diagnosis (Ministry of Education), and Key Laboratory of Analytical Science and Technology of Hebei Province, College of Chemistry and Environment Science, Hebei University, Baoding 071002, China.

Peking University Health Science Center, Beijing 100191, China.

出版信息

Anal Chem. 2020 Sep 15;92(18):12137-12144. doi: 10.1021/acs.analchem.9b04926. Epub 2020 Aug 26.

DOI:10.1021/acs.analchem.9b04926
PMID:32844652
Abstract

Photostable and bright organic dyes emitting in the near-infrared region are highly desirable for long-term dynamic bioimaging. Herein, we report a synthetic approach to build novel methoxy modified Si-rhodamine (SiRMO) dyes by introducing the methoxybenzene on the xanthene moiety. The brightness of SiRMO increased from 2300 M cm (SiRMO-0) to 49000 M cm (SiRMO-2) when the substituent 2,5-dimethoxybenzene was replaced with 2,6-dimethoxybenzene. Moreover, the stability of SiRMO-2 was significantly improved due to the steric hindrance protection of the two methoxy groups on the ninth carbon atom of the xanthene. After fast cellular uptake, the SiRMO dyes selectively stained the mitochondria with a low background in live cultured cells and primary neurons. The high brightness and stability of SiRMO-2 significantly improved the capability of monitoring mitochondria dynamic processes in living cells under super-resolution conditions. Moreover, with the fluorescence nanoscopy techniques, we observed the structure of mitochondrial cristae and mitochondria fission, fusion, and apoptosis with a high temporal resolution. Under two-photon illumination, SiRMO-2 showed also enhanced two-photon brightness and stability, which are important for imaging in thick tissue.

摘要

发射近红外区域的光稳定和明亮的有机染料非常适合长期动态生物成像。在此,我们报告了一种通过在香豆素部分引入甲氧基苯来构建新型甲氧基修饰的 Si-罗丹明(SiRMO)染料的合成方法。当取代基 2,5-二甲氧基苯被 2,6-二甲氧基苯取代时,SiRMO 的亮度从 2300 M cm(SiRMO-0)增加到 49000 M cm(SiRMO-2)。此外,由于香豆素第九位碳原子上的两个甲氧基的空间位阻保护,SiRMO-2 的稳定性得到了显著提高。快速细胞摄取后,SiRMO 染料选择性地对活培养细胞和原代神经元中的线粒体进行染色,背景低。SiRMO-2 的高亮度和稳定性显著提高了在超分辨率条件下监测活细胞中线粒体动态过程的能力。此外,利用荧光纳米镜技术,我们以高时间分辨率观察到线粒体嵴和线粒体裂变、融合和凋亡的结构。在双光子激发下,SiRMO-2 还表现出增强的双光子亮度和稳定性,这对于厚组织成像很重要。

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