AI Article Synopsis

  • Ion channels are essential for cell function, and their dysfunction can lead to diseases like epilepsy and diabetes, often treated with drugs that target these channels.
  • High throughput screening (HTS) allows for efficient testing of ion channel activity, but traditional methods like patch clamping, while precise, are slow and costly.
  • New technologies combining the advantages of patch clamping with HTS are being developed, which could revolutionize drug discovery by making it easier to screen and optimize compounds targeting ion channels.

Article Abstract

Proper function of ion channels is crucial for all living cells. Ion channel dysfunction may lead to a number of diseases, so-called channelopathies, and a number of common diseases, including epilepsy, arrhythmia, and type II diabetes, are primarily treated by drugs that modulate ion channels. A cornerstone in current drug discovery is high throughput screening assays which allow examination of the activity of specific ion channels though only to a limited extent. Conventional patch clamp remains the sole technique with sufficiently high time resolution and sensitivity required for precise and direct characterization of ion channel properties. However, patch clamp is a slow, labor-intensive, and thus expensive, technique. New techniques combining the reliability and high information content of patch clamping with the virtues of high throughput philosophy are emerging and predicted to make a number of ion channel targets accessible for drug screening. Specifically, genuine HTS parallel processing techniques based on arrays of planar silicon chips are being developed, but also lower throughput sequential techniques may be of value in compound screening, lead optimization, and safety screening. The introduction of new powerful HTS electrophysiological techniques is predicted to cause a revolution in ion channel drug discovery.

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