| Literature DB >> 32997976 |
Toshiyuki Kowada1, Tomomi Watanabe2, Yuta Amagai3, Rong Liu2, Momo Yamada4, Hiroto Takahashi3, Toshitaka Matsui1, Kenji Inaba1, Shin Mizukami5.
Abstract
Fluorescent Zn2+ probes used for the quantitative analysis of labile Zn2+ concentration ([Zn2+]) in target organelles are crucial for understanding the role of Zn2+ in biological processes. Although several fluorescent Zn2+ probes have been developed to date, there is still a lack of consensus concerning the [Zn2+] in intracellular organelles. In this study, we describe the development of ZnDA-1H, a small-molecule fluorescent probe for Zn2+, which exhibits less pH sensitivity, high Zn2+ selectivity, and large fluorescence enhancement upon binding to Zn2+. Through protein labeling technology, ZnDA-1H was precisely targeted in various intracellular organelles, such as the nucleus, mitochondria, endoplasmic reticulum, and Golgi apparatus. ZnDA-1H exhibited a reversible fluorescence response toward labile Zn2+ in these organelles in live cells. Using this probe, the [Zn2+] in the Golgi apparatus was estimated to be 25 ± 1 nM, suggesting that labile Zn2+ plays a physiological role in the secretory pathway.Entities:
Keywords: Golgi apparatus; Zn(2+); fluorescence imaging; quantitative analysis
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Year: 2020 PMID: 32997976 DOI: 10.1016/j.chembiol.2020.09.003
Source DB: PubMed Journal: Cell Chem Biol ISSN: 2451-9448 Impact factor: 8.116