A lysosome targetable and acidic pH-activated fluorescent probe for two-photon imaging of hydrogen sulfide in live cells and animals†

IF 2.6 3区 化学 Q2 CHEMISTRY, ANALYTICAL
YuJia Fu, XiaoFeng Guo and Hong Wang
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Abstract

The design strategy of targeted fluorescent probes usually involves modifying the probes with organelle-targeting groups, which then guide the probes to enter specific organelles by the traction of the targeting groups. However, the targeting ability of subcellular localization groups is not perfect, and the target analytes are not specifically distributed within the cells. Therefore, designing novel molecular fluorescent probes for highly specific and selective detection of target analytes within specific organelles is an important research direction that deserves attention. Although multiple high-efficiency lysosomal localization fluorescent probes for H2S have been developed, the pH range for the fluorescence response of these probes to H2S does not match the specific acidic range of the lysosome very well. In this work, by analyzing the relationship between the structures of the pH-responsive groups and the response range, excellent acidic pH-activated lysosome-localized fluorescent probes Lyso-NP-DS and Lyso-NP-NBD with a better performance have been developed. After the reaction with H2S, the fluorescence activation pH ranges of their derivatives were between 2.5 and 5.5, 3.0 and 5.5, respectively. However, this could not only solve the problem of insufficient matching between the pH activation range for the fluorescence response to H2S and the specific acidic range within the lysosome, but it also shows the characteristics of two-photon excitation and high sensitivity. This effectively avoids the background interference and extracellular fluorescence interference in the lysosome, and an accurate and efficient detection of H2S within the lysosome is achieved.

Abstract Image

用于活细胞和动物硫化氢双光子成像的溶酶体靶和酸性ph激活荧光探针。
靶向荧光探针的设计策略通常包括用细胞器靶向基团修饰探针,然后在靶向基团的牵引下引导探针进入特定的细胞器。然而,亚细胞定位群的靶向能力并不完善,靶分析物在细胞内没有特异性分布。因此,设计新型分子荧光探针对特定细胞器内的目标分析物进行高特异性、高选择性的检测是一个值得关注的重要研究方向。虽然已经开发出多种高效的H2S溶酶体定位荧光探针,但这些探针对H2S的荧光响应的pH范围与溶酶体的特定酸性范围并不匹配。本研究通过分析ph响应基团的结构与响应范围的关系,开发出性能较好的酸性ph活化溶酶体定位荧光探针Lyso-NP-DS和Lyso-NP-NBD。与H2S反应后,其衍生物的荧光活化pH范围分别在2.5 ~ 5.5、3.0 ~ 5.5之间。然而,这不仅可以解决H2S荧光响应的pH活化范围与溶酶体内特定酸性范围不匹配的问题,而且还显示出双光子激发和高灵敏度的特点。这有效地避免了溶酶体内的背景干扰和细胞外荧光干扰,实现了对溶酶体内H2S的准确、高效检测。
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来源期刊
Analytical Methods
Analytical Methods CHEMISTRY, ANALYTICAL-FOOD SCIENCE & TECHNOLOGY
CiteScore
5.10
自引率
3.20%
发文量
569
审稿时长
1.8 months
期刊介绍: Early applied demonstrations of new analytical methods with clear societal impact
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