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Bioinspired Chemosensor with Configuration-Dependent Affinity for Localized Tracking of Labile Zn2+ during Neuronal
Jian Chen1,2, Huixia Feng1,2, Chi Zhan1,2
1Beijing National Laboratory for Molecular Sciences, CAS Key Laboratories of Analytical Chemistry for Living Biosystems and Organic Solids, CAS Research/Education Center for Excellence in Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.
None:
Homeostasis and transportation of labile Zn2+ across neuronal membranes are of great importance for biological functions, in which molecular tools are urgently demanded to understand the mechanism of actions in depth. Here, we report a zinc-specific fluorescence-switchable chemosensor (trans T-P) for the targetable tracing of labile Zn2+ in live nerve cells. The molecular design was inspired by the coordination structure in the catalytic centers of metalloenzymes. The strong coordination and response to Zn2+ were demonstrated to be stereochemistry-sensitive, in which only the trans conformer has ultrahigh affinity, selectivity, and sensitivity. Benefited from its amphiphilic and phosphate-bearing molecular structure, trans T-P is readily cell membrane permeable and achieves preferential accumulation in the near-membrane region, enabling regionally specific localization and imaging of labile Zn2+ at the intracellular side of plasma membranes. Provided with these unique properties, trans T-P achieved an in situ visualization of labile Zn2+ fluctuations during neuronal differentiation. The targeted sorting and tracking highlight the prominence of trans T-P in monitoring Zn2+ spatiotemporal dynamics for understanding the actions of labile Zn2+ in nerve functions and development.
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