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We present an in-depth analysis of ChiSCAT, a recently introduced interferometric microscopy scheme to detect recurring micromotion events in cells. Experimentally, we demonstrate that illumination with low-coherence sources can greatly improve the robustness of the scheme to vibrations. We analyze the theoretical performance of ChiSCAT under various noise models, particularly photon shot noise and noise dominated by cellular motions other than the signal. We finally propose ways to improve performance, especially in a setting dominated by cell motions, and conclude with an outlook on potential future directions.
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http://dx.doi.org/10.1364/AO.547639 | DOI Listing |
We present an in-depth analysis of ChiSCAT, a recently introduced interferometric microscopy scheme to detect recurring micromotion events in cells. Experimentally, we demonstrate that illumination with low-coherence sources can greatly improve the robustness of the scheme to vibrations. We analyze the theoretical performance of ChiSCAT under various noise models, particularly photon shot noise and noise dominated by cellular motions other than the signal.
View Article and Find Full Text PDFNano Lett
October 2024
Institute of Physics, University of Rostock, 18059 Rostock, Germany.
There is considerable evidence that action potentials are accompanied by "intrinsic optical signals", such as a nanometer-scale motion of the cell membrane. Here we present ChiSCAT, a technically simple imaging scheme that detects such signals with interferometric sensitivity. ChiSCAT combines illumination by a aotic speckle pattern and interferometric scattering microscopy () to sensitively detect motion in any direction.
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