Related Experiment Video
Updated: Jun 1, 2026

Atomic Force Microscopy Imaging and Force Spectroscopy of Supported Lipid Bilayers
Published on: July 22, 2015
High-speed atomic force microscopy of membrane and membrane protein dynamics
Abeer Alshammari1, Bashra Mahamed2, George R Heath3
1School of Physics & Astronomy, Bragg Centre for Materials Research, University of Leeds, Leeds, UK; Department of Physics, College of Science, University of Hafr Al Batin, Hafr Al Batin, Saudi Arabia.
None:
High-speed atomic force microscopy (HS-AFM) enables direct nanometer-resolution visualization of single molecules and molecular assemblies in real-time and under physiological conditions, providing unique insights into how membranes and membrane proteins move and interact within native lipid environments. Recent methodological advances and integration with complementary techniques have extended HS-AFM to increasingly complex, physiologically relevant systems, bridging gaps between high-resolution static structural methods and low-resolution functional dynamics. Here, we highlight how HS-AFM has changed our understanding of membrane organization, protein conformational dynamics, and lipid-protein coupling. By capturing transient events inaccessible to ensemble approaches, HS-AFM is transforming our ability to connect structural snapshots with functional behavior, advancing dynamic structural biology.
More Related Videos
Related Concept Videos
Atomic Force Microscopy
The AFM Probe
The probe is regarded as the heart of any AFM setup and comprises the...
Protein Dynamics in Living Cells
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...
Studying the Cytoskeleton
Protein Diffusion in the Membrane

