Nature CommunicationsBiochemistryPeer-reviewed journal article
MAASTY: A (dis)ordered copolymer for structural determination of human membrane proteins in native nanodiscs
Ciara Frances PughiD, Lukas P. FeileniD, Dušan ŽivkovićiD, Kaia Fiil PræstegaardiD, Charalampos SiderisiD, Neil Jean BorthwickiD, Casper de LichtenbergiD, Jani Reddy BollaiD, Anton A. A. AutzeniD, Henriette Elisabeth AutzeniD
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. Amphiphilicity, length, and composition influence the performance of copolymers, 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 with 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.
- organism: human
- assay: cryo-EM
- research focus: protein structure prediction
- approach: experimental assay
- Citations
- 9
- FWCI
- 2.16
- Field percentile
- top 11%
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Characterization of divalent cation interactions with AASTY native nanodiscs
M. Timcenko, A. A. A. Autzen, H. E. Autzen·bioRxiv·Oct 7, 2021
- Self-assembly of polymer-encased lipid nanodiscs and membrane protein reconstitution
B. Sahoo, T. Genjo, … A. Ramamoorthy·bioRxiv·Feb 28, 2019
- Membrane Proteins at Scale: Automated Copolymer Nanodisc Purification for Structure and Function
Philipp T. Hanisch, Lea Marie Esser, … Jan Kubicek·bioRxiv·Sep 5, 2025
- Mass Photometry of Membrane Proteins
A. Olerinyova, A. Sonn Segev, … P. Kukura·bioRxiv·Feb 28, 2020
- A Bioinspired Glycopolymer for Capturing Membrane Proteins in Native-Like Lipid-Bilayer Nanodiscs
B. Danielczak, M. Rasche, … S. Keller·bioRxiv·Mar 31, 2021
- The bigger picture: global analysis of solubilization performance of classical detergents versus new synthetic polymers utilizing shotgun proteomics
S. Mueller, J. Kubicek, … J.-W. Lackmann·bioRxiv·Jul 11, 2023