Functional Insertion of the Light-Induced Ion Pump KR2 into Block Copolymer Membranes

High Resolution Image Download MS PowerPoint Slide Light-driven membrane proteins are attractive functional elements for biohybrid membranes, as they enable direct conversion of light energy into ion gradients. While microbial rhodopsins have been extensively studied in lipid bilayers, their controlled incorporation into synthetic polymer membranes remains challenging. Here, we investigate the reconstitution of the light-driven proton and sodium pump Krokinobacter eikastus rhodopsin 2 (KR2) into amphiphilic block copolymer membranes using a mild detergent-assisted strategy. KR2 and a C-terminal GFP fusion variant were incorporated into both solid-supported planar membranes and polymersomes under low concentrations of n -dodecyl-β- d -maltopyranoside. Membrane stability and protein incorporation were characterized using surface-sensitive and fluorescence-based techniques, while ion transport activity was assessed in polymersomes. The GFP fusion enabled quantitative assessment of membrane association and insertion behavior. Reconstituted KR2 variants retained light-driven ion transport activity in polymersomes. This straightforward approach supports the development of biohybrid systems with potential for light-driven ion transport, sensing, and energy-conversion applications.

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Publication Details

Journal
Biomacromolecules
Published
2026-07-16
DOI
https://doi.org/10.1021/acs.biomac.6c00738
Primary Topic
Photoreceptor and optogenetics research
Type
article
Field-Weighted Citation Impact
0.00

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article

Functional Insertion of the Light-Induced Ion Pump KR2 into Block Copolymer Membranes

Piotr Jaśko, Cornelia G. Palivan, Cora‐Ann Schoenenberger, Richard A. Kammerer et al.
Biomacromolecules
Photoreceptor and optogenetics research
article

Functional Insertion of the Light-Induced Ion Pump KR2 into Block Copolymer Membranes

Piotr Jaśko, Cornelia G. Palivan, Cora‐Ann Schoenenberger, Richard A. Kammerer, Maryame Bina, Moritz S. Muthwill, Daniel Frey
article en

Abstract

High Resolution Image Download MS PowerPoint Slide Light-driven membrane proteins are attractive functional elements for biohybrid membranes, as they enable direct conversion of light energy into ion gradients. While microbial rhodopsins have been extensively studied in lipid bilayers, their controlled incorporation into synthetic polymer membranes remains challenging. Here, we investigate the reconstitution of the light-driven proton and sodium pump Krokinobacter eikastus rhodopsin 2 (KR2) into amphiphilic block copolymer membranes using a mild detergent-assisted strategy. KR2 and a C-terminal GFP fusion variant were incorporated into both solid-supported planar membranes and polymersomes under low concentrations of n -dodecyl-β- d -maltopyranoside. Membrane stability and protein incorporation were characterized using surface-sensitive and fluorescence-based techniques, while ion transport activity was assessed in polymersomes. The GFP fusion enabled quantitative assessment of membrane association and insertion behavior. Reconstituted KR2 variants retained light-driven ion transport activity in polymersomes. This straightforward approach supports the development of biohybrid systems with potential for light-driven ion transport, sensing, and energy-conversion applications.

Biomacromolecules
University of Basel (CH), Paul Scherrer Institute (CH), Center for Life Sciences (CN), Institute of Molecular and Clinical Ophthalmology Basel (CH), Swiss Nanoscience Institute
Universität Basel, Paul Scherrer Institut, Swiss Nanoscience Institute
Affordable and clean energy
Openalex Percentile: Top 13%
Photoreceptor and optogenetics research
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