Automatic deep learning-driven label-free image-guided patch clamp system

Patch clamp recording of neurons is a labor-intensive and time-consuming procedure. Here, we demonstrate a tool that fully automatically performs electrophysiological recordings in label-free tissue slices. The automation covers the detection of cells in label-free images, calibration of the micropi...

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Published inNature communications Vol. 12; no. 1; pp. 936 - 11
Main Authors Koos, Krisztian, Oláh, Gáspár, Balassa, Tamas, Mihut, Norbert, Rózsa, Márton, Ozsvár, Attila, Tasnadi, Ervin, Barzó, Pál, Faragó, Nóra, Puskás, László, Molnár, Gábor, Molnár, József, Tamás, Gábor, Horvath, Peter
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 10.02.2021
Nature Publishing Group
Nature Portfolio
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ISSN2041-1723
2041-1723
DOI10.1038/s41467-021-21291-4

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Summary:Patch clamp recording of neurons is a labor-intensive and time-consuming procedure. Here, we demonstrate a tool that fully automatically performs electrophysiological recordings in label-free tissue slices. The automation covers the detection of cells in label-free images, calibration of the micropipette movement, approach to the cell with the pipette, formation of the whole-cell configuration, and recording. The cell detection is based on deep learning. The model is trained on a new image database of neurons in unlabeled brain tissue slices. The pipette tip detection and approaching phase use image analysis techniques for precise movements. High-quality measurements are performed on hundreds of human and rodent neurons. We also demonstrate that further molecular and anatomical analysis can be performed on the recorded cells. The software has a diary module that automatically logs patch clamp events. Our tool can multiply the number of daily measurements to help brain research. Patch clamp recording of neurons is slow and labor-intensive. Here the authors present a method for automated deep learning driven label-free image guided patch clamp physiology to perform measurements on hundreds of human and rodent neurons.
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ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-021-21291-4