Stress propagation through membranes
Stress propagation through membranes
Disciplines
Other Technical Sciences (25%); Biology (25%); Chemistry (25%); Clinical Medicine (25%)
Keywords
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Membrane Channels,
Electrophysiology,
Mechanosensation,
Single Molecule Fluorescence,
Single Molecule Microscopy,
Membrane Diffusion
Central to the perception of tactile or acoustic stimuli is the conversion of mechanical stimuli into electrical signals that can be processed by the nervous system. Responsible for the conversion are so- called mechanosensitive channels in the membrane of specialized cells. When open, these channels conduct ions, i.e., they generate an electrical signal. It is currently unclear whether the channel opening is mediated by contact with other proteins, more precisely with proteins of the cytoskeleton. According to an alternative hypothesis, the mechanical stimulus could also be transmitted directly by the surrounding membrane to the channel. We will test this hypothesis by isolating such channels from their natural environment and incorporating them into simple lipid bilayers. To generate mechanical stimuli, we use photo-switchable lipids. If the stimuli were to be conducted by the membrane, we would detect channel opening utilizing current measurements even if the area containing the light-switched lipids was located at some distance from the mechanosensitive channels. Contrary results would indicate that direct contact between cytoskeleton and channel is required.
This project demonstrated that light-much like flipping a switch-can be converted into an electrical signal in cells that are not naturally light-sensitive. This is achieved using specially designed light-sensitive lipids ("photolipids") that change their shape upon illumination. This structural change modulates the activity of natural ion channels in the membrane-without the need for genetic modification. By introducing light responsiveness externally, the approach offers new strategies for controlling biological processes and holds potential for biomedical research, such as investigating signal transmission or developing novel therapies.
- Universität Linz - 100%
Research Output
- 29 Citations
- 7 Publications
- 1 Methods & Materials
- 2 Datasets & models
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2025
Title UTILIZING PHOTOSWITCHABLE LIPIDS TO PHOTOREGULATE FACILITATED ION TRANSPORT ACROSS MEMBRANES Type PhD Thesis Author Rohit Yadav -
2025
Title Clear Native Gel Electrophoresis for the Purification of Fluorescently Labeled Membrane Proteins in Native Nanodiscs DOI 10.1101/2025.03.21.644524 Type Preprint Author Ezsias B -
2025
Title Enhanced Site-Specific Fluorescent Labeling of Membrane Proteins Using Native Nanodiscs. DOI 10.3390/biom15020254 Type Journal Article Author Ezsias B Journal Biomolecules -
2025
Title Modulation of Kv Channel Gating by Light-Controlled Membrane Thickness. DOI 10.3390/biom15050744 Type Journal Article Author Pfeffermann J Journal Biomolecules -
2024
Title Using photolipids to trigger channel activity by light DOI 10.1016/j.bpj.2023.11.275 Type Journal Article Author Pfeffermann J Journal Biophysical Journal -
2021
Title Biophysical Reviews’ “Meet the Councilor Series”—a profile of Peter Pohl DOI 10.1007/s12551-021-00897-4 Type Journal Article Author Pohl P Journal Biophysical Reviews Pages 839-844 Link Publication -
2021
Title Photoswitching of model ion channels in lipid bilayers DOI 10.1016/j.jphotobiol.2021.112320 Type Journal Article Author Pfeffermann J Journal Journal of Photochemistry and Photobiology B: Biology Pages 112320 Link Publication
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2021
Link
Title Photoresponsive lipid-based modulation of membrane protein activity DOI 10.1101/2025.01.13.632814 Type Technology assay or reagent Public Access Link Link
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2025
Link
Title Enhanced site-specific fluorescent labeling of membrane proteins using native nanodiscs DOI 10.5281/zenodo.14620507 Type Database/Collection of data Public Access Link Link -
2025
Link
Title Modulation of Kv Channel Gating by Light-Controlled Membrane Thickness DOI 10.5281/zenodo.15465224 Type Database/Collection of data Public Access Link Link