What makes MAASTY different?

MAASTY is a methacrylic acid–styrene copolymer series designed for direct extraction of membrane proteins from native membranes into lipid nanodiscs. By systematically varying the methacrylic acid (MAA) content from 40 to 60 mol%, we give you a toolkit to find the optimal hydrophilic–hydrophobic balance for your specific membrane protein and lipid system — without detergent.

MAASTY nanodisc concept: membrane protein extraction and reconstitution workflow
Reconstitution strategies for native lipid nanodiscs. Top path: conventional reconstitution requires detergent solubilisation of the target membrane protein, followed by addition of exogenous lipid and scaffold polymer or belt protein, yielding reconstituted nanodiscs with a defined but artificial lipid composition. Bottom path: MAASTY enables single-step direct extraction — the copolymer is added directly to a membrane preparation and co-solubilises the target protein together with its native lipid annulus, yielding native nanodiscs that retain the endogenous lipid composition. Right: chemical structures of AASTY (poly(acrylic acid-co-styrene)) and MAASTY (poly(methacrylic acid-co-styrene)), differing by a single methyl group on each hydrophilic monomer unit. Pugh, Feilen, Autzen et al., Nat. Commun. 2025.

The MAASTY Composition Series

MAASTY40 · RP-001

40 mol% MAA · 60 mol% styrene

The most hydrophobic variant. MAASTY40's high styrene content makes it well-suited for membrane proteins embedded in cholesterol-rich or hydrophobic-heavy bilayers, where stronger hydrophobic interactions with the belt polymer support efficient extraction.

MAASTY45 · RP-002

45 mol% MAA · 55 mol% styrene

A moderately hydrophobic variant with broad membrane compatibility. MAASTY45 is a strong starting point for cholesterol-containing eukaryotic membranes and has shown good performance across diverse lipid compositions.

MAASTY50 · RP-003

50 mol% MAA · 50 mol% styrene

The balanced midpoint of the series — equal MAA and styrene content. MAASTY50 provides a useful reference point for comparisons with the published AASTY literature and is a strong general-purpose starting point for new membrane protein targets.

MAASTY55 · RP-004

55 mol% MAA · 45 mol% styrene

A moderately hydrophilic variant. MAASTY55 suits membrane proteins in lipid environments rich in charged headgroups, where a more hydrophilic belt polymer promotes efficient nanodisc formation and protein stability.

MAASTY60 · RP-005

60 mol% MAA · 40 mol% styrene

The most hydrophilic variant. MAASTY60 is designed for membrane systems dominated by anionic or polar lipids, or for membrane proteins that are destabilised by highly hydrophobic polymer belts.

Why Composition Matters

Most commercial nanodisc polymers are sold at a single fixed composition — leaving researchers with no systematic way to optimise extraction for their membrane system. The MAASTY series is designed to change that. By sweeping MAA content from 40 to 60 mol% in matched 5 mol% steps, we give you a controlled compositional axis to screen across.


Replacing acrylic acid with methacrylic acid adds a methyl group to each hydrophilic monomer on the backbone. This increases the overall hydrophobicity of the polymer and results in a less ordered monomer distribution compared to AASTY — properties that translate directly into superior extraction efficiency for cholesterol-rich eukaryotic membranes.


Monomer composition profiles and run-length distributions for MAASTY vs AASTY
Monomer sequence statistics for MAASTY and AASTY. Left: instantaneous MAA monomer fraction as a function of chain position during MAASTY synthesis at initial feed compositions of 40–65 mol% MAA — the near-flat profiles indicate uniform incorporation throughout the chain for all variants. Centre: equivalent data for AASTY (acrylic acid feed fractions 40–65 mol%), showing systematic composition drift that reflects the higher reactivity ratio of the acrylic acid–styrene pair. Right: run-length distributions for MAASTY (average run length 1.68) and AASTY (average run length 1.28); the longer runs in MAASTY confirm a statistically less ordered, more disordered monomer placement — consistent with the "(dis)ordered" descriptor in the paper title and the distinct nanodisc-forming behaviour of the two polymers. Pugh, Feilen, Autzen et al., Nat. Commun. 2025.

3.5 Å Cryo-EM of Human TRPM4

MAASTY nanodiscs preserve endogenous lipids — including cholesterol — and show enrichment of phosphatidylinositol, reflecting the native membrane environment rather than a reconstituted approximation. As demonstrated in Nature Communications (2025), this native lipid retention enables high-quality structural biology directly from cellular membranes.


3.5 Å cryo-EM structure of human TRPM4 in MAASTY nanodiscs
Cryo-EM structure of human TRPM4 determined in MAASTY native nanodiscs at 3.5 Å global resolution. Top row, left to right: composite cryo-EM density map viewed from the extracellular face showing the tetrameric assembly; side-view map with the surrounding nanodisc belt visible; and ribbon representation coloured by subunit. Bottom row: close-up of the transmembrane helical bundle with fitted density mesh illustrating map quality at the protein–lipid interface; and detail of the selectivity filter region with modelled density and coordinated ions. The structure was determined directly from native cellular membranes without detergent solubilisation, retaining the endogenous cholesterol and phosphatidylinositol lipid environment. Pugh, Feilen, Autzen et al., Nat. Commun. 2025.

Technical Specifications

All MAASTY products are synthesised by RAFT polymerisation with defined molecular weight. Products are delivered lyophilised from 50 mM HEPES, pH 8.0, and ship at room temperature. Reconstitution to a 10% w/v stock requires addition of ultrapure water only.


Each batch is characterised by GPC (molecular weight), ¹H-NMR (composition verification), and a nanodisc formation assay prior to release.

Key Publications


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