MAASTY: a (dis)ordered copolymer for structural determination of human membrane proteins in native nanodiscs

Amphiphilic copolymers capable of extracting membrane proteins directly from cellular membranes into "native nanodiscs" offer a simplified approach for preparing membrane proteins in lipid nanodiscs compared to approaches that rely on detergent. Copolymer amphiphilicity, length, and composition influence their performance, in addition to the protein itself and the purification conditions used. Here, we report a copolymer composed of methacrylic acid and styrene, which we term MAASTY, leveraging the inherent monomer reactivity ratios to create an anionic copolymer with a statistical distribution of monomers. We show that MAASTY can be used for high-resolution structural determination of a human membrane protein by single particle cryo-electron microscopy, preserving endogenous lipids including cholesterol and exhibiting an enrichment of phosphatidylinositol. Moreover, MAASTY copolymers effectively solubilize a broad range of lipid species and a wide range of different, eukaryotic membrane proteins from mammalian cells. We find that MAASTY copolymers are promising as effective solubilizers of membrane proteins and offer a chemical platform for structural and functional characterization of membrane proteins in native nanodiscs.

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Publication Details

Journal
Nature Communications
Published
2025-12-10
DOI
https://doi.org/10.1038/s41467-025-66208-7
Citations
1
Primary Topic
Lipid Membrane Structure and Behavior
Type
article
Field-Weighted Citation Impact
0.81

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article

MAASTY: a (dis)ordered copolymer for structural determination of human membrane proteins in native nanodiscs

Neil Jean Borthwick, Henriette Elisabeth Autzen, Ciara Frances Pugh, Casper de Lichtenberg et al.
1 citations
Nature Communications
Lipid Membrane Structure and Behavior
0.81
article

MAASTY: a (dis)ordered copolymer for structural determination of human membrane proteins in native nanodiscs

Neil Jean Borthwick, Henriette Elisabeth Autzen, Ciara Frances Pugh, Casper de Lichtenberg, Jani Reddy Bolla, Lukas P. Feilen, Anton A. A. Autzen, Dušan Živković, Kaia Fiil Præstegaard, Charalampos Sideris
article en
1 citations

Abstract

Amphiphilic copolymers capable of extracting membrane proteins directly from cellular membranes into "native nanodiscs" offer a simplified approach for preparing membrane proteins in lipid nanodiscs compared to approaches that rely on detergent. Copolymer amphiphilicity, length, and composition influence their performance, in addition to the protein itself and the purification conditions used. Here, we report a copolymer composed of methacrylic acid and styrene, which we term MAASTY, leveraging the inherent monomer reactivity ratios to create an anionic copolymer with a statistical distribution of monomers. We show that MAASTY can be used for high-resolution structural determination of a human membrane protein by single particle cryo-electron microscopy, preserving endogenous lipids including cholesterol and exhibiting an enrichment of phosphatidylinositol. Moreover, MAASTY copolymers effectively solubilize a broad range of lipid species and a wide range of different, eukaryotic membrane proteins from mammalian cells. We find that MAASTY copolymers are promising as effective solubilizers of membrane proteins and offer a chemical platform for structural and functional characterization of membrane proteins in native nanodiscs.

Nature CommunicationsVol. 16(1)
University of Copenhagen (DK), University of Oxford (GB), Technical University of Denmark (DK)
Novo Nordisk, Novo Nordisk Fonden
Openalex Percentile: Top 21%
Lipid Membrane Structure and Behavior
0.81
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