Genetically Encoded Sensors to Elucidate Spatial Distribution of Cellular Zinc

• Published in: The Journal of biological chemistry Vol. 284; no. 24; pp. 16289 - 16297
• Main Authors: Dittmer, Philip J., Miranda, Jose G., Gorski, Jessica A., Palmer, Amy E.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 12-06-2009; American Society for Biochemistry and Molecular Biology
• Subjects: Animals; Calibration; Cell Membrane - metabolism; Cytosol - metabolism; Fluorescence Resonance Energy Transfer - methods; Fluorescent Dyes - pharmacokinetics; Glutamic Acid - pharmacology; HeLa Cells; Hippocampus - cytology; Homeostasis - physiology; Humans; Mechanisms of Signal Transduction; Mitochondria - metabolism; Neurons - cytology; Neurons - metabolism; Rats; Rats, Sprague-Dawley; Transfection; Zinc - metabolism
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M900501200

Transition metals are essential enzyme cofactors that are required for a wide range of cellular processes. Paradoxically, whereas metal ions are essential for numerous cellular processes, they are also toxic. Therefore cells must tightly regulate metal accumulation, transport, distribution, and export. Improved tools to interrogate metal ion availability and spatial distribution within living cells would greatly advance our understanding of cellular metal homeostasis. In this work, we present genetically encoded sensors for Zn2+ based on the principle of fluorescence resonance energy transfer. We also develop methodology to calibrate the probes within the cellular environment. To identify both sources of and sinks for Zn2+, these sensors are genetically targeted to specific locations within the cell, including cytosol, plasma membrane, and mitochondria. Localized probes reveal that mitochondria contain an elevated pool of Zn2+ under resting conditions that can be released into the cytosol upon glutamate stimulation of hippocampal neurons. We also observed that Zn2+ is taken up into mitochondria following glutamate/Zn2+ treatment and that there is heterogeneity in both the magnitude and kinetics of the response. Our results suggest that mitochondria serve as a source of and a sink for Zn2+ signals under different cellular conditions.