Evidence map›Paper›PMID 40709568›Full record

ArticleJournal of the American Chemical Society2025

Design and Synthesis of Hetero-Bicephalic Detergents for Native Mass Spectrometry of Membrane Proteins.

Jing-Yuan Chang, Djavdat Azizov, Vikki N Shinde, Sangho D Yun, Robert L Rider, Yun Zhu, Hanieh Bahramimoghaddam, Michael Lynn, David H Russell, Lei Fang and 1 more

Abstract read
In one paragraph

Article in Journal of the American Chemical Society, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Jing-Yuan ChangDepartment of Chemistry, Texas A&M University, College Station, Texas 77843, United States.
Djavdat AzizovDepartment of Chemistry, Texas A&M University, College Station, Texas 77843, United States.
Vikki N ShindeDepartment of Chemistry, Texas A&M University, College Station, Texas 77843, United States.
Sangho D YunDepartment of Chemistry, Texas A&M University, College Station, Texas 77843, United States.
Robert L RiderDepartment of Chemistry, Texas A&M University, College Station, Texas 77843, United States.ORCID 0000-0002-7894-4920
Yun ZhuDepartment of Chemistry, Texas A&M University, College Station, Texas 77843, United States.
Hanieh BahramimoghaddamDepartment of Chemistry, Texas A&M University, College Station, Texas 77843, United States.
Michael LynnDepartment of Chemistry, Texas A&M University, College Station, Texas 77843, United States.
David H RussellDepartment of Chemistry, Texas A&M University, College Station, Texas 77843, United States.ORCID 0000-0003-0830-3914
Lei FangDepartment of Chemistry, Texas A&M University, College Station, Texas 77843, United States.ORCID 0000-0003-4757-5664
Arthur LaganowskyDepartment of Chemistry, Texas A&M University, College Station, Texas 77843, United States.ORCID 0000-0001-5012-5547

Funding

Understanding the role of lipids in structure and function of membrane proteinsRM1GM145416 · NIGMS · TEXAS A&M UNIVERSITY · PI Erin S Baker, Arthur D Laganowsky · 2022 to 2026
$7.4M
Native Mass Spectrometry Guided Structural Biology CenterRM1GM149374 · NIGMS · OHIO STATE UNIVERSITY · PI Vicki H. Wysocki · 2023 to 2026
$5.0M
Innovative Native Ion Mobility Approaches for Transformational Measurements in Structural BiologyR01GM138863 · NIGMS · TEXAS A&M UNIVERSITY · PI CLOWERS, BRIAN, LAGANOWSKY, ARTHUR D · 2020 to 2023
$1.2M
Developing new tools to probe membrane protein-lipid interactions for biomedical applicationsR01GM139876 · NIGMS · TEXAS A&M UNIVERSITY · PI LAGANOWSKY, ARTHUR D · 2021 to 2024
$1.2M
NIGMS NIH HHS R01 GM138863NIGMS NIH HHS R01 GM139876NIGMS NIH HHS RM1 GM145416NIGMS NIH HHS RM1 GM149374
6 · The paper itself

Abstract

Native mass spectrometry is playing a central role in characterizing the noncovalent interactions of membrane proteins, enabling the discovery of lipids that regulate membrane protein function and modulate interactions with other molecules. The use of specialized charge-reducing detergents and/or molecular additives is critical to mitigate overactivation during native MS to facilitate proper analysis. Here, we present the design and synthesis of a new class of dual-headgroup detergents featuring two distinct hydrophilic moieties. One headgroup, the spermine moiety, is designed to promote lower charge states of membrane proteins, thereby enhancing the preservation of labile complexes in the mass spectrometer. The other hydrophilic headgroup─either a maltoside or a tetraethylene glycol moiety─is commonly found in traditional detergents used for the extraction and solubilization of membrane protein complexes. Using a diverse set of membrane proteins varying in size, topology, and oligomeric state, we demonstrate that these novel dual-headgroup detergents exhibit exceptional charge-reducing properties, particularly when introduced to membrane proteins solubilized in different detergents. Additionally, we highlight their effectiveness in preserving the complex of a G-protein-coupled receptor with a nanobody that selectively binds to its active state. Collectively, these high-performance detergents advance the rational design of detergents for native MS and expand the capabilities for studying membrane proteins in diverse biochemical environments.

Indexed as

DetergentsMembrane ProteinsHydrophobic and Hydrophilic InteractionsMass SpectrometryDetergentsMembrane Proteins

Identifiers

PMID40709568
PMCPMC12327940

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.