Developing High-Throughput Assays to Analyze and Screen Electrophysiological Phenotypes.
Ion channels represent nearly a quarter of all targets that currently available medications modulate, and their dysfunction underlies increasing number of human diseases. Functional analysis of ion channels have traditionally been a bottleneck in large-scale analyses. Recent technological breakthroughs in automated planar electrophysiology have democratized the technique to enable high-throughput patch clamping at scale. In this chapter, we describe the methodology to perform a phenotypic screen on voltage-gated calcium channels across many different genetic coding variations and against small-molecule modulators. We first describe the procedures to establish inducible heterologous ion channel expression in HEK293 cells, where each cell incorporates one copy of a target protein cDNA-a step that is critical for producing stable and consistent expression of ion channels. We then describe the experimental and analytical methods for analyzing the function of ion channels using high-throughput planar electrophysiology.
Duke Scholars
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Volume
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Related Subject Headings
- Workflow
- Patch-Clamp Techniques
- Ion Channel Gating
- Humans
- High-Throughput Screening Assays
- HEK293 Cells
- Gene Expression
- Electrophysiological Phenomena
- Drug Discovery
- Developmental Biology
Citation
DOI
Publication Date
Volume
Start / End Page
Related Subject Headings
- Workflow
- Patch-Clamp Techniques
- Ion Channel Gating
- Humans
- High-Throughput Screening Assays
- HEK293 Cells
- Gene Expression
- Electrophysiological Phenomena
- Drug Discovery
- Developmental Biology