Quantification of lysosomal labile Zn2+and monitoring of Zn2+efflux using a small-molecule-protein hybrid fluorescent probe

被引:0
|
作者
Du, Yuyin [1 ]
Kowada, Toshiyuki [2 ,3 ,4 ]
Sung, Eunhye [4 ]
Liu, Rong [2 ]
Soloviev, Andrei [3 ]
Matsui, Toshitaka [2 ,3 ,4 ]
Mizukami, Shin [2 ,3 ,4 ]
机构
[1] Tohoku Univ, Fac Sci, Dept Chem, 6-3 Aramaki Aza Aoba,Aoba Ku, Sendai, Miyagi 9808578, Japan
[2] Tohoku Univ, Inst Multidisciplinary Res Adv Mat, 2-1-1 Katahira,Aoba Ku, Sendai, Miyagi 9808577, Japan
[3] Tohoku Univ, Grad Sch Life Sci, 2-1-1 Katahira,Aoba Ku, Sendai, Miyagi 9808577, Japan
[4] Tohoku Univ, Grad Sch Sci, Dept Chem, 6-3 Aramaki Aza Aoba,Aoba Ku, Sendai, Miyagi 9808578, Japan
关键词
Zinc; Lysosome; Fluorescence imaging; TRPMLs; HaloTag; Protein labeling; ZINC; RELEASE; INDICATOR; SENSOR;
D O I
10.1016/j.jinorgbio.2024.112811
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Lysosomal labile Zn2+ levels have been unclear. By targeting a small-molecule fluorescent Zn2+ probe, ZnDA-3H, to lysosomes via VAMP7-Halo, the lysosomal labile Zn2+ concentration was determined to be 1.9 nM in HeLa cells. Furthermore, ZnDA-3H enabled direct visualization of the Zn2+ efflux from the lysosomes to cytosol upon TRPMLs activation.
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页数:5
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