Journal
NATURE METHODS
Volume 13, Issue 4, Pages 341-344Publisher
NATURE PUBLISHING GROUP
DOI: 10.1038/NMETH.3769
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Funding
- US National Institutes of Health [1R01GM079238, 1R01GM098859]
- German Academic Exchange Service (DAAD)
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Single-molecule fluorescence microscopy is uniquely suited for detecting transient molecular recognition events, yet achieving the time resolution and statistics needed to realize this potential has proven challenging. Here we present a single-molecule imaging and analysis platform using scientific complementary metal-oxide semiconductor (sCMOS) detectors that enables imaging of 15,000 individual molecules simultaneously at millisecond rates. This system enabled the detection of previously obscured processes relevant to the fidelity mechanism in protein synthesis.
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