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

Journal: Nature communications
PMID:

Abstract

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.

Authors

  • Krisztian Koos
    Synthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
  • Gáspár Oláh
    MTA-SZTE Research Group for Cortical Microcircuits of the Hungarian Academy of Sciences, Department of Physiology, Anatomy and Neuroscience, University of Szeged, Szeged, Hungary.
  • Tamas Balassa
    Biological Research Centre of the Hungarian Academy of Sciences, Szeged, Hungary.
  • Norbert Mihut
    MTA-SZTE Research Group for Cortical Microcircuits of the Hungarian Academy of Sciences, Department of Physiology, Anatomy and Neuroscience, University of Szeged, Szeged, Hungary.
  • Márton Rózsa
    MTA-SZTE Research Group for Cortical Microcircuits of the Hungarian Academy of Sciences, Department of Physiology, Anatomy and Neuroscience, University of Szeged, Szeged, Hungary.
  • Attila Ozsvár
    MTA-SZTE Research Group for Cortical Microcircuits of the Hungarian Academy of Sciences, Department of Physiology, Anatomy and Neuroscience, University of Szeged, Szeged, Hungary.
  • Ervin Tasnadi
    Synthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
  • Pál Barzó
    Department of Neurosurgery, University of Szeged, Szeged, Hungary.
  • Nóra Faragó
    MTA-SZTE Research Group for Cortical Microcircuits of the Hungarian Academy of Sciences, Department of Physiology, Anatomy and Neuroscience, University of Szeged, Szeged, Hungary.
  • László Puskás
    Laboratory of Functional Genomics, Institute of Genetics, Biological Research Centre, Szeged, Hungary.
  • Gabor Molnar
    The ATLAS Institute, University of Colorado, Boulder, CO, United States.
  • Jozsef Molnar
    Synthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
  • Gábor Tamás
    MTA-SZTE Research Group for Cortical Microcircuits of the Hungarian Academy of Sciences, Department of Physiology, Anatomy and Neuroscience, University of Szeged, Szeged, Hungary.
  • Péter Horváth
    Department of Pulmonology, Semmelweis University, Budapest, Hungary.