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Updated: Jun 14, 2026

A Technique for Stabilizing Membrane Proteins in Nanodiscs
Published on: April 30, 2026
Amphipols, nanodiscs, and fluorinated surfactants: three nonconventional approaches to studying membrane proteins in
1Laboratoire de Physico-Chimie Moléculaire des Protéines Membranaires, Unité Mixte de Recherche 7099, Centre National de la Recherche Scientifique and Université Paris-7 Denis Diderot, Institut de Biologie Physico-Chimique, F-75005 Paris, France. jean-luc.popot@ibpc.fr
Abstract:
Membrane proteins (MPs) are usually handled in aqueous solutions as protein/detergent complexes. Detergents, however, tend to be inactivating. This situation has prompted the design of alternative surfactants that can be substituted for detergents once target proteins have been extracted from biological membranes and that keep them soluble in aqueous buffers while stabilizing them. The present review focuses on three such systems: Amphipols (APols) are amphipathic polymers that adsorb onto the hydrophobic transmembrane surface of MPs; nanodiscs (NDs) are small patches of lipid bilayer whose rim is stabilized by amphipathic proteins; fluorinated surfactants (FSs) resemble detergents but interfere less than detergents do with stabilizing protein/protein and protein/lipid interactions. The structure and properties of each of these three systems are described, as well as those of the complexes they form with MPs. Their respective usefulness, constraints, and prospects for functional and structural studies of MPs are discussed.
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