Amyloid β 1-42 Can Form Ion Channels as Small as Gramicidin in Model Lipid Membranes

Yue Xu1, Irina Bukhteeva1,2, Yurii Potsiluienko1

  • 1Department of Physics and Astronomy, University of Waterloo, Waterloo, ON N2L 3G1, Canada.

Membranes
|July 25, 2025
PubMed

Insights

Amyloid-beta 1-42 oligomers form small, dynamic ion channels in lipid membranes, contributing to Alzheimer's Disease pathology. This research clarifies their membrane damage mechanism and cytotoxicity.

Area of Science:

  • Neuroscience
  • Biophysics
  • Molecular Biology

Background:

  • Amyloid-beta 1-42 (Aβ1-42) oligomers are key in Alzheimer's Disease (AD) pathology.
  • Aβ1-42 oligomers damage cellular membranes via complex mechanisms, including pore and ion channel formation.

Purpose of the Study:

  • To investigate the membrane damage induced by Aβ1-42 oligomers.
  • To compare the channel-forming activity of Aβ1-42 with gramicidin.

Main Methods:

  • Black lipid membrane (BLM) electrophysiology.
  • Utilized lipid membranes composed of DPPC, POPC, and cholesterol.

Main Results:

  • Aβ1-42 oligomers induced ion channels in lipid membranes, similar to gramicidin.
  • These channels had an average inner diameter < 5 Å and short retention times, indicating high dynamism.
  • Observed membrane damage in DPPC, POPC, and cholesterol lipid mixtures.

Conclusions:

  • Aβ1-42 oligomers form small, dynamic ion channels in lipid membranes.
  • Findings provide insights into Aβ-induced membrane damage and cytotoxicity in Alzheimer's Disease.
  • Supports and extends the amyloid-beta channelopathy hypothesis in AD pathogenesis.

Related Concept Videos

Amyloid Fibrils03:03

Amyloid Fibrils

Amyloid fibrils are aggregates of misfolded proteins.  Under most circumstances, misfolded proteins are either refolded by chaperone proteins or degraded by the proteasome. However, in the case of a mutation or a disease, these proteins can accumulate to form large clusters and often further assemble to form elongated fibers, called fibrils. 
Amyloid deposits were observed as early as 1639 in the liver and the spleen.   In 1854, Rudolph Virchow performed iodine staining,...
9.9K
Fluid Mosaic Model01:19

Fluid Mosaic Model

Scientists identified the plasma membrane in the 1890s and its principal chemical components (lipids and proteins) by 1915. The model for plasma membrane structure, proposed in 1935 by Hugh Davson and James Danielli, was the first model to be widely accepted in the scientific community. The model was based on the plasma membrane's "railroad track" appearance in early electron micrographs. Davson and Danielli theorized that the plasma membrane's structure resembled a sandwich...
12.9K
Mechanisms of Membrane Domain Formation00:59

Mechanisms of Membrane Domain Formation

Different physical properties of lipids and proteins allow them to localize and form distinct islands or domains in the membrane. Some membrane domains are formed due to protein-protein interactions, whereas others are formed due to the presence of specific lipids such as sphingolipids and sterols—for example, large proteins, such as bacteriorhodopsin, aggregate and create distinct domains.
Another mechanism for membrane domain formation involves membrane proteins interacting with...
3.2K
Multi-pass Transmembrane Proteins and &#946;-barrels01:09

Multi-pass Transmembrane Proteins and β-barrels

In multi-pass transmembrane proteins, the polypeptide chain crosses the membrane more than once. The transmembrane polypeptide chain either forms an α-helix or β-strand structure. α-Helix containing multi-pass transmembrane proteins are ubiquitous, whereas β-strand containing ones are mainly found in gram-negative bacteria, mitochondria, and chloroplasts.
α-Helix containing multi-pass transmembrane proteins
Multi-pass transmembrane proteins such as...
5.5K