Evidence map›Paper›PMID 39886581›Full record

ArticleJACS Au2025

Native Mass Spectrometry Captures the Conformational Plasticity of Proteins with Low-Complexity Domains.

Hannah Osterholz, Alexander Stevens, Mia L Abramsson, Dilraj Lama, Klaus Brackmann, Anna Rising, Arne Elofsson, Erik G Marklund, Sebastian Deindl, Axel Leppert and 1 more

Abstract read
In one paragraph

Article in JACS Au, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
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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.

Hannah OsterholzDepartment of Cell and Molecular Biology, Uppsala University, 751 24 Uppsala, Sweden.ORCID https://orcid.org/0009-0006-3481-1540
Alexander StevensDepartment of Cell and Molecular Biology, Uppsala University, 751 24 Uppsala, Sweden.
Mia L AbramssonDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institutet, 171 65 Solna, Sweden.ORCID https://orcid.org/0000-0002-8184-0145
Dilraj LamaDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institutet, 171 65 Solna, Sweden.
Klaus BrackmannDepartment of Cell and Molecular Biology, Science for Life Laboratory, Uppsala University, 751 24 Uppsala, Sweden.
Anna RisingDepartment of Animal Biosciences, Swedish University of Agricultural Sciences, 750 07 Uppsala, Sweden.ORCID https://orcid.org/0000-0002-1872-1207
Arne ElofssonDepartment of Biochemistry and Biophysics and Science for Life Laboratory, Stockholm University, 171 21 Solna, Sweden.
Erik G MarklundDepartment of Chemistry-BMC, Uppsala University, 751 23 Uppsala, Sweden.ORCID https://orcid.org/0000-0002-9804-5009
Sebastian DeindlDepartment of Cell and Molecular Biology, Science for Life Laboratory, Uppsala University, 751 24 Uppsala, Sweden.
Axel LeppertDepartment of Cell and Molecular Biology, Uppsala University, 751 24 Uppsala, Sweden.ORCID https://orcid.org/0000-0001-6223-3350
Michael LandrehDepartment of Cell and Molecular Biology, Uppsala University, 751 24 Uppsala, Sweden.ORCID https://orcid.org/0000-0002-7958-4074

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Disordered regions are an important functional feature of many multidomain proteins. A prime example is proteins in membraneless organelles, which contain folded domains that engage in specific interactions and disordered low-complexity (LC) domains that mediate liquid-liquid phase separation. Studying these complex architectures remains challenging due to their conformational variability. Native mass spectrometry (nMS) is routinely employed to analyze conformations and interactions of folded or disordered proteins; however, its ability to analyze proteins with disordered LC domains has not been investigated. Here, we analyze the ionization and conformational states of designed model proteins that recapitulate key features of proteins found in membraneless organelles. Our results show that charge state distributions (CSDs) in nMS reflect partial disorder regardless of the protein sequence, providing insights into their conformational plasticity and interactions. By applying the same CSD analysis to a spider silk protein fragment, we find that interactions between folded domains that trigger silk assembly simultaneously induce conformational changes in the LC domains. Lastly, using intact nucleosomes, we demonstrate that CSDs are a good predictor for the disorder content of complex native assemblies. We conclude that nMS reliably informs about the conformational landscape of proteins with LC domains, which is crucial for understanding protein condensates in cellular environments.

Identifiers

PMID39886581
PMCPMC11775691

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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.