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本文引用的文献

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Cell-specific gain modulation by synaptically released zinc in cortical circuits of audition.突触释放的锌在听觉皮层回路中对细胞的特异性调节。
Elife. 2017 Sep 9;6:e29893. doi: 10.7554/eLife.29893.
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The zinc paradigm for metalloneurochemistry.金属神经化学的锌范式。
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An Endoperoxide Reactivity-Based FRET Probe for Ratiometric Fluorescence Imaging of Labile Iron Pools in Living Cells.基于内过氧化物反应性的荧光共振能量转移探针用于活细胞中不稳定铁池的比率荧光成像。
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AMPA receptor inhibition by synaptically released zinc.突触释放的锌对α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)受体的抑制作用
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Modulation of extrasynaptic NMDA receptors by synaptic and tonic zinc.突触和持续性锌对突触外NMDA受体的调节
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6
Quantitative mapping of zinc fluxes in the mammalian egg reveals the origin of fertilization-induced zinc sparks.定量绘制哺乳动物卵中的锌流图谱揭示了受精诱导锌火花的起源。
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Photocaged DNAzymes as a general method for sensing metal ions in living cells.光笼控脱氧核酶作为一种检测活细胞中金属离子的通用方法。
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Genetically-encoded FRET-based sensors for monitoring Zn(2+) in living cells.用于监测活细胞中锌离子(Zn²⁺)的基于荧光共振能量转移(FRET)的基因编码传感器。
Metallomics. 2015 Feb;7(2):258-66. doi: 10.1039/c4mt00179f.
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Fluorescent sensors for measuring metal ions in living systems.用于测量生物系统中金属离子的荧光传感器。
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Tris(2-pyridylmethyl)amine (TPA) as a membrane-permeable chelator for interception of biological mobile zinc.三(2-吡啶甲基)胺(TPA)作为一种膜通透性螯合剂,用于拦截生物体内的可移动锌离子。
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用于检测可移动锌的光活化传感器。

Photoactivatable Sensors for Detecting Mobile Zinc.

机构信息

Department of Chemistry, Massachusetts Institute of Technology , 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States.

Pittsburgh Hearing Research Center, Department of Otolaryngology, University of Pittsburgh , 3501 Fifth Avenue, Pittsburgh, Pennsylvania 15261, United States.

出版信息

J Am Chem Soc. 2018 Feb 14;140(6):2020-2023. doi: 10.1021/jacs.7b12766. Epub 2018 Jan 31.

DOI:10.1021/jacs.7b12766
PMID:29384658
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5935517/
Abstract

Fluorescent sensors for mobile zinc are valuable for studying complex biological systems. Because these sensors typically bind zinc rapidly and tightly, there has been little temporal control over the activity of the probe after its application to a sample. The ability to control the activity of a zinc sensor in vivo during imaging experiments would greatly improve the time resolution of the measurement. Here, we describe photoactivatable zinc sensors that can be triggered with short pulses of UV light. These probes are prepared by functionalizing a zinc sensor with protecting groups that render the probe insensitive to metal ions. Photoinduced removal of the protecting groups restores the binding site, allowing for zinc-responsive changes in fluorescence that can be observed in live cells and tissues.

摘要

用于检测游离锌的荧光传感器对于研究复杂的生物系统非常有用。由于这些传感器通常能够快速且紧密地结合锌离子,因此在将探针应用于样品后,对探针的活性几乎无法进行时间控制。如果能够在活体成像实验中控制锌传感器的活性,将极大地提高测量的时间分辨率。在这里,我们描述了可通过短脉冲紫外光触发的光活化锌传感器。这些探针是通过用保护基团对锌传感器进行功能化来制备的,这些保护基团使探针对金属离子不敏感。光诱导去除保护基团恢复了结合位点,使得能够在活细胞和组织中观察到对锌响应的荧光变化。