# Celebrating 50 Years of Single-Channel Recording with the Patch Clamp

**Authors:** Luigi Catacuzzeno, Fabio Franciolini

PMC · DOI: 10.1007/s00232-025-00362-3 · The Journal of Membrane Biology · 2025-09-19

## TL;DR

This paper celebrates the 50th anniversary of the patch clamp technique, which allowed scientists to observe individual ion channels in real time, revolutionizing the study of cell membranes.

## Contribution

The paper highlights the historical significance and lasting impact of the patch clamp technique in ion channel research.

## Key findings

- The patch clamp technique enabled the first recordings of single-channel currents in native ion channels.
- It provided detailed insights into ion channel behavior, including conformational changes and kinetic properties.
- The technique resolved a decade-long scientific debate about the existence of ion channels on cell membranes.

## Abstract

Fifty years ago, Erwin Neher and Bert Sakmann published a Nature paper on their recording of discrete, step-like currents of a few picoamps passing through individual acetylcholine receptor channels of frog muscle fibers. This observation, the first on native channels, immediately ended the decade-long dispute about the presence of ion channels on cell membranes by convincing even the most reluctant scientists that this was indeed the case. More importantly, however, the ability to record single-channel currents revolutionized the study of ion channels because it enabled scientists to observe their behavior individually in real time. We could observe them change conformation, jumping from the closed state to the open state and back again. This level of detail provided an unprecedented understanding of the gating mechanisms, conductance, and kinetic properties of channels. This retrospective illustrates the scientific context in which all of this occurred as well as its immediate and current impact on the investigation of ion channels.

## Full-text entities

- **Genes:** PKD2L1 (polycystin 2 like 1, transient receptor potential cation channel) [NCBI Gene 9033] {aka PCL, PKD2L, PKDL, TRPP3}
- **Diseases:** neurological disorders (MESH:D009461), pain (MESH:D010146), cardiac arrhythmias (MESH:D001145)
- **Chemicals:** benzoate (MESH:D001565), lipid (MESH:D008055), propionate (MESH:D011422), suberyldicholine (MESH:C009335), ACh (MESH:D000109), Na+ (MESH:D012964), nitrate (MESH:D009566), Ca2+ (-), Cl- (MESH:D002713), Cation (MESH:D002412), TEA (MESH:D019789), K+ (MESH:D011188), acetate (MESH:D000085), TTX (MESH:D013779), aspartate (MESH:D001224), SCN- (MESH:C031760), oxygen (MESH:D010100), amphotericin B (MESH:D000666), F (MESH:D005461), NaCl (MESH:D012965), water (MESH:D014867), KCl (MESH:D011189), Br (MESH:D001966), hydrogen (MESH:D006859)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** GH3 — Rattus norvegicus (Rat), Rat pituitary gland neoplasm, Cancer cell line (CVCL_0273), BOSC 23 — Homo sapiens (Human), Transformed cell line (CVCL_4401)

## Full text

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## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12602605/full.md

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Source: https://tomesphere.com/paper/PMC12602605