Abstract
Electrochemical impedance spectroscopy is a crucial tool for the detection and study of various biological substances, from DNA and proteins to viruses and bacteria. It does not require any labelling species, and methods based on it have been developed to study cellular processes (such as cell spreading, adhesion, invasion, toxicology and mobility). However, data have so far lacked spatial information, which is essential for investigating heterogeneous processes and imaging high-throughput microarrays. Here, we report an electrochemical impedance microscope based on surface plasmon resonance that resolves local impedance with submicrometre spatial resolution. We have used an electrochemical impedance microscope to monitor the dynamics of cellular processes (apoptosis and electroporation of individual cells) with millisecond time resolution. The high spatial and temporal resolution makes it possible to study individual cells, but also resolve subcellular structures and processes without labels, and with excellent detection sensitivity (~2 pS). We also describe a model that simulates cellular and electrochemical impedance microscope images based on local dielectric constant and conductivity.
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Acknowledgements
The authors thank the National Institutes of Health (NIH, R21RR026235) and National Science Foundation (NSF, CHE-0554786) for support.
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K.F. performed initial impedance imaging of cells. W.W. carried out the measurement and data analysis presented here. X.S. contributed to numerical simulation and prepared gold chips. S.E., V.J.N. and P.W. helped with cell culture. K.F. and U.P. developed imaging processing software. W.W., K.F. and S.W. designed and set up the experiment. N.J.T. conceived the experiment and model simulation, and wrote the paper.
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Wang, W., Foley, K., Shan, X. et al. Single cells and intracellular processes studied by a plasmonic-based electrochemical impedance microscopy. Nature Chem 3, 249–255 (2011). https://doi.org/10.1038/nchem.961
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DOI: https://doi.org/10.1038/nchem.961
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