Wu Xue, Zhang Ruixin, Li Ying, Gai Yitong, Feng Tingting, Kou Junjie, Kong Fanpeng, Li Lu, Tang Bo
College of Chemistry, Chemical Engineering and Materials Science, Collaborative Innovation Center of Functionalized Probes for Chemical Imaging in Universities of Shandong, Key Laboratory of Molecular and Nano Probes, Ministry of Education, Shandong Normal University, Jinan 250014, People's Republic of China.
Anal Chem. 2023 May 16;95(19):7611-7619. doi: 10.1021/acs.analchem.3c00436. Epub 2023 May 3.
Mitochondrial viscosity affects metabolite diffusion and mitochondrial metabolism and is associated with many diseases. However, the accuracy of mitochondria-targeting fluorescent probes in measuring viscosity is unsatisfactory because these probes can diffuse from mitochondria during mitophagy with a decreased mitochondrial membrane potential (MMP). To avoid this problem, by incorporating different alkyl side chains into dihydroxanthene fluorophores (denoted as ), we developed six near-infrared (NIR) probes for the accurate detection of mitochondrial viscosity, and the sensitivity to viscosity and the mitochondrial targeting and anchoring capability of these probes increased by increasing the alkyl chain length. Among them, had a highly selective response to viscosity variations with minimum interference from polarity, pH, and other biologically relevant species. Furthermore, was used to monitor the mitochondrial viscosity changes of HeLa cells treated by ionophores (nystatin, monensin) or under starvation conditions. We hope that this mitochondrial targeting and anchoring strategy based on increasing the alkyl chain length will be a general strategy for the accurate detection of mitochondrial analytes, enabling the accurate study of mitochondrial functions.
线粒体粘度影响代谢物扩散和线粒体代谢,并与许多疾病相关。然而,靶向线粒体的荧光探针在测量粘度方面的准确性并不理想,因为这些探针在有丝分裂期间会随着线粒体膜电位(MMP)降低而从线粒体中扩散出来。为避免此问题,通过将不同的烷基侧链引入二氢蒽荧光团(表示为 ),我们开发了六种用于准确检测线粒体粘度的近红外(NIR)探针,并且这些探针对粘度的敏感性以及线粒体靶向和锚定能力随着烷基链长度的增加而增强。其中, 对粘度变化具有高度选择性响应,受极性、pH值和其他生物相关物质的干扰最小。此外, 用于监测经离子载体(制霉菌素、莫能菌素)处理或在饥饿条件下的HeLa细胞的线粒体粘度变化。我们希望这种基于增加烷基链长度的线粒体靶向和锚定策略将成为准确检测线粒体分析物的通用策略,从而能够准确研究线粒体功能。