Zinspy sensors with enhanced dynamic range for imaging neuronal cell zinc uptake and mobilization

被引:225
作者
Nolan, Elizabeth M.
Ryu, Jubin W.
Jaworski, Jacek
Feazell, Rodney P.
Sheng, Morgan
Lippard, Stephen J. [1 ]
机构
[1] MIT, Dept Chem, Cambridge, MA 02139 USA
[2] MIT, Picower Inst Learning & Memory, Cambridge, MA 02139 USA
[3] MIT, RIKEN, Neurosci Res Ctr, Cambridge, MA 02139 USA
[4] MIT, Howard Hughes Med Inst, Cambridge, MA 02139 USA
[5] Int Inst Mol & Cell Biol, Lab Mol & Cellular Neurobiol, PL-02109 Warsaw, Poland
关键词
D O I
10.1021/ja065759a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Thiophene moieties were incorporated into previously described Zinspy (ZS) fluorescent Zn(II) sensor motifs (Nolan, E. M.; Lippard, S. J. Inorg. Chem. 2004, 43, 8310-8317) to provide enhanced fluorescence properties, low-micromolar dissociation constants for Zn(II), and improved Zn(II) selectivity. Halogenation of the xanthenone and benzoate moieties of the fluorescein platform systematically modulates the excitation and emission profiles, pH-dependent fluorescence, Zn(II) affinity, and Zn(II) complexation rates, offering a general strategy for tuning multiple properties of xanthenone- based metal ion sensors. Extensive biological studies in cultured cells and primary neuronal cultures demonstrate 2-{6-hydroxy-3-oxo- 4,5-bis[(pyridin-2-ylmethylthiophen-2-ylmethylamino)methyl]-3H-xanthen-9-yl}benzoic acid (ZS5) to be a versatile imaging tool for detecting Zn(II) in vivo. ZS5 localizes to the mitochondria of HeLa cells and allows visualization of glutamate-mediated Zn(II) uptake in dendrites and Zn(II) release resulting from nitrosative stress in neurons.
引用
收藏
页码:15517 / 15528
页数:12
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