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A genetically encoded far-red fluorescent indicator for imaging synaptically released Zn(2+)

Synaptic zinc ion (Zn(2+)) has emerged as a key neuromodulator in the brain. However, the lack of research tools for directly tracking synaptic Zn(2+) in the brain of awake animals hinders our rigorous understanding of the physiological and pathological roles of synaptic Zn(2+). In this study, we de...

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Detalles Bibliográficos
Autores principales: Wu, Tianchen, Kumar, Manoj, Zhang, Jing, Zhao, Shengyu, Drobizhev, Mikhail, McCollum, Mason, Anderson, Charles T., Wang, Ying, Pokorny, Antje, Tian, Xiaodong, Zhang, Yiyu, Tzounopoulos, Thanos, Ai, Hui-wang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9977179/
https://www.ncbi.nlm.nih.gov/pubmed/36857451
http://dx.doi.org/10.1126/sciadv.add2058
Descripción
Sumario:Synaptic zinc ion (Zn(2+)) has emerged as a key neuromodulator in the brain. However, the lack of research tools for directly tracking synaptic Zn(2+) in the brain of awake animals hinders our rigorous understanding of the physiological and pathological roles of synaptic Zn(2+). In this study, we developed a genetically encoded far-red fluorescent indicator for monitoring synaptic Zn(2+) dynamics in the nervous system. Our engineered far-red fluorescent indicator for synaptic Zn(2+) (FRISZ) displayed a substantial Zn(2+)-specific turn-on response and low-micromolar affinity. We genetically anchored FRISZ to the mammalian extracellular membrane via a transmembrane (TM) ⍺ helix and characterized the resultant FRISZ-TM construct at the mammalian cell surface. We used FRISZ-TM to image synaptic Zn(2+) in the auditory cortex in acute brain slices and awake mice in response to electric and sound stimuli, respectively. Thus, this study establishes a technology for studying the roles of synaptic Zn(2+) in the nervous system.