Gao Yue, Liu Xia, Li Wei, Chen Yuncong, Zhu Shitai, Yan Qinglong, Geng Shanshan, Zhang Jichao, Guan Yong, Li Qian, Jia Sisi, Wang Lihua, Li Jiang, He Weijiang, Fan Chunhai, Guo Zijian, Zhu Ying
CAS Key Laboratory of Interfacial Physics and Technology, Shanghai Institute of Applied Physics, Chinese Academy of Sciences, Shanghai 201800, China.
Institute of Materiobiology, College of Sciences, Shanghai University, Shanghai 200444, China.
Natl Sci Rev. 2024 Sep 12;11(11):nwae307. doi: 10.1093/nsr/nwae307. eCollection 2024 Nov.
Abnormal levels of zinc ions within endo-lysosomes have been implicated in the progression of Alzheimer's disease (AD), yet the detection of low-concentration zinc ions at the organelle level remains challenging. Here we report the design of an endo-lysosome-targeted fluorescent reporter, Znluor, for imaging endogenous zinc ions. Znluor is constructed from an amphiphilic DNA framework (DNF) with programmable size and shape, which can encapsulate zinc-responsive fluorophores within its hydrophobic nanocavity. We find that the tetrahedral DNFs of 20 bp in the edge length are effectively located within endo-lysosomes, which can detect zinc ions with a detection limit of ∼31.9 nM (a sensitivity that is ∼2.5 times that of the free fluorophore). Given the organelle-targeting ability and high zinc sensitivity of Znluor, we employ it to detect endogenous endo-lysosomal zinc ions in neuron cells. We monitor the dynamics of zinc levels in AD model cells and zebrafish, corroborating the positive correlation between zinc levels and AD hallmarks including Aβ aggregates and learning/memory impairments. Our study provides a generalizable strategy for organelle-specific theranostic applications.
内溶酶体内锌离子水平异常与阿尔茨海默病(AD)的进展有关,但在细胞器水平检测低浓度锌离子仍然具有挑战性。在此,我们报告了一种用于成像内源性锌离子的内溶酶体靶向荧光报告分子Znluor的设计。Znluor由具有可编程大小和形状的两亲性DNA框架(DNF)构建而成,其可以在其疏水纳米腔内封装锌响应荧光团。我们发现边长为20 bp的四面体DNF有效地定位于内溶酶体内,其可以检测锌离子,检测限约为31.9 nM(灵敏度约为游离荧光团的2.5倍)。鉴于Znluor的细胞器靶向能力和高锌灵敏度,我们用它来检测神经元细胞中的内源性内溶酶体锌离子。我们监测了AD模型细胞和斑马鱼中锌水平的动态变化,证实了锌水平与包括Aβ聚集体和学习/记忆障碍在内的AD特征之间的正相关。我们的研究为细胞器特异性治疗诊断应用提供了一种可推广的策略。