4.8 Article

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

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 128, Issue 48, Pages 15517-15528

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja065759a

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Funding

  1. NCRR NIH HHS [1S10RR-13886-01] Funding Source: Medline
  2. NIGMS NIH HHS [R01 GM065519, GM65519, R01 GM065519-01] Funding Source: Medline

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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.

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