Abstract
We introduce a new approach to monitor the dynamics and spatial patterns of biological molecular assemblies. Our molecular imaging method relies on plasmonic gold nanoparticles as point-like detectors and requires no labeling of the molecules. We show spatial resolution of up to 5 μm and 30 ms temporal resolution, which is comparable to wide-field fluorescence microscopy, while requiring only readily available gold nanoparticles and a dark-field optical microscope. We demonstrate the method on MinDE proteins attaching to and detaching from lipid membranes of different composition for 24 h. We foresee our new imaging method as an indispensable tool in advanced molecular biology and biophysics laboratories around the world.
MeSH terms
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Adenosine Triphosphatases / chemistry
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Adenosine Triphosphatases / metabolism*
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Cardiolipins / chemistry
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Cell Cycle Proteins / chemistry
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Cell Cycle Proteins / metabolism*
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Escherichia coli / chemistry
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Escherichia coli Proteins / chemistry
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Escherichia coli Proteins / metabolism*
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Gold / chemistry
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Lipid Bilayers / chemistry
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Lipid Bilayers / metabolism
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Metal Nanoparticles / chemistry*
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Microscopy / methods
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Nanotubes / chemistry
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Phosphatidylcholines / chemistry
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Phosphatidylglycerols / chemistry
Substances
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Cardiolipins
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Cell Cycle Proteins
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Escherichia coli Proteins
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Lipid Bilayers
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MinE protein, E coli
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Phosphatidylcholines
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Phosphatidylglycerols
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1,2-dioleoyl-sn-glycero-3-phosphoglycerol
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Gold
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Adenosine Triphosphatases
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MinD protein, E coli
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1,2-oleoylphosphatidylcholine