Autonomous patch-clamp robot for functional characterization of neurons in vivo: development and application to mouse visual cortex

Author:

Holst Gregory L.1ORCID,Stoy William2ORCID,Yang Bo1,Kolb Ilya2,Kodandaramaiah Suhasa B.3,Li Lu4,Knoblich Ulf4,Zeng Hongkui4,Haider Bilal2,Boyden Edward S.567,Forest Craig R.1

Affiliation:

1. George W. Woodruff School of Mechanical Engineering, Georgia Institute of Technology, Atlanta, Georgia

2. Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology, Atlanta, Georgia

3. Department of Mechanical Engineering, University of Minnesota, Minneapolis, Minnesota

4. Allen Institute for Brain Science, Seattle, Washington

5. Media Arts and Sciences, Massachusetts Institute of Technology, Cambridge, Massachusetts

6. McGovern Institute, Massachusetts Institute of Technology, Cambridge, Massachusetts

7. Koch Institute, Massachusetts Institute of Technology, Cambridge, Massachusetts

Abstract

Patch clamping is the gold standard measurement technique for cell-type characterization in vivo, but it has low throughput, is difficult to scale, and requires highly skilled operation. We developed an autonomous robot that can acquire multiple consecutive patch-clamp recordings in vivo. In practice, 40 pipettes loaded into a carousel are sequentially filled and inserted into the brain, localized to a cell, used for patch clamping, and disposed. Automated visual stimulation and electrophysiology software enables functional cell-type classification of whole cell-patched cells, as we show for 37 cells in the anesthetized mouse in visual cortex (V1) layer 5. We achieved 9% yield, with 5.3 min per attempt over hundreds of trials. The highly variable and low-yield nature of in vivo patch-clamp recordings will benefit from such a standardized, automated, quantitative approach, allowing development of optimal algorithms and enabling scaling required for large-scale studies and integration with complementary techniques. NEW & NOTEWORTHY In vivo patch-clamp is the gold standard for intracellular recordings, but it is a very manual and highly skilled technique. The robot in this work demonstrates the most automated in vivo patch-clamp experiment to date, by enabling production of multiple, serial intracellular recordings without human intervention. The robot automates pipette filling, wire threading, pipette positioning, neuron hunting, break-in, delivering sensory stimulus, and recording quality control, enabling in vivo cell-type characterization.

Funder

NSF Integrative Graduate Education Research Traineeship

Georgia Institute of Technology Presidential Fellowship

NSF Graduate Research Fellowship

NIH Computational Neuroscience Training Grant

Georgia Tech Neural Engineering Center Seed Grant

NIH Grant

Georgia Tech Institute for Bioengineering and Biosciences Junior Faculty Award

Georgia Tech Technology Fee Fund

Georgia Tech Invention Studio

George W. Woodruff School of Mechanical Engineering

Paul G. Allen and Jody Patton, Allen Institute for Brain Science

Publisher

American Physiological Society

Subject

Physiology,General Neuroscience

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