Evidence map›Paper›PMID 39941124›Full record

ArticleInternational journal of molecular sciences2025

Structural Characteristics and Properties of the RNA-Binding Protein hnRNPK at Multiple Physical States.

Quang D Le, Amanda Lewis, Alice Dix-Matthews, Philippe Ringler, Anthony Duff, Andrew E Whitten, Rob Atkin, Manuel Brunner, Diwei Ho, K Swaminathan Iyer and 3 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 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. Review
  2. Article
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

13 authors.

Quang D LeSchool of Molecular Sciences, University of Western Australia, Crawley, WA 6009, Australia.ORCID 0009-0003-1253-7438
Amanda LewisCenter for Cellular Imaging and NanoAnalytics (C-CINA), Biozentrum, University of Basel, 4001 Basel, Switzerland.
Alice Dix-MatthewsSchool of Molecular Sciences, University of Western Australia, Crawley, WA 6009, Australia.
Philippe RinglerCenter for Cellular Imaging and NanoAnalytics (C-CINA), Biozentrum, University of Basel, 4001 Basel, Switzerland.ORCID 0000-0003-4346-5089
Anthony DuffAustralian Centre for Neutron Scattering, Australian Nuclear Science and Technology Organisation, New Illawarra Road, Lucas Heights, NSW 2234, Australia.
Andrew E WhittenAustralian Centre for Neutron Scattering, Australian Nuclear Science and Technology Organisation, New Illawarra Road, Lucas Heights, NSW 2234, Australia.
Rob AtkinSchool of Molecular Sciences, University of Western Australia, Crawley, WA 6009, Australia.
Manuel BrunnerSchool of Molecular Sciences, University of Western Australia, Crawley, WA 6009, Australia.
Diwei HoSchool of Molecular Sciences, University of Western Australia, Crawley, WA 6009, Australia.
K Swaminathan IyerSchool of Molecular Sciences, University of Western Australia, Crawley, WA 6009, Australia.
Andrew C MarshallSchool of Molecular Sciences, University of Western Australia, Crawley, WA 6009, Australia.ORCID 0000-0002-9770-4594
Archa H FoxSchool of Molecular Sciences, University of Western Australia, Crawley, WA 6009, Australia.
Charles S BondSchool of Molecular Sciences, University of Western Australia, Crawley, WA 6009, Australia.

Funding

Australian Research Council ARC DP160102435, LE120100092 and LE140100096National Health and Medical Research Council NHMRC APP1147496Vietnam International Education Development (VIED) and the University of Western Australia Vietnam International Education Development (VIED) and the University of Western Australia
6 · The paper itself

Abstract

Heterogeneous nuclear ribonucleoprotein K (hnRNPK) is an RNA-binding protein containing low-complexity domains (LCDs), which are known to regulate protein behavior under stress conditions. This study demonstrates the ability to control hnRNPK's transitions into four distinct material states-monomer, soluble aggregate, liquid droplet, and fibrillar hydrogel-by modulating environmental factors such as temperature and protein concentration. Importantly, the phase-separated and hydrogel states are newly identified for eGFP-hnRNPK, marking a significant advancement in understanding its material properties. A combination of biophysical techniques, including DLS and SEC-LS, were used to further characterize hnRNPK in monomeric and soluble aggregate states. Structural methods, such as SANS, SAXS, and TEM, revealed the elongated morphology of the hnRNPK monomer. Environmental perturbations, such as decreased temperature or crowding agents, drove hnRNPK into phase-separated or gel-like states, each with distinct biophysical characteristics. These novel states were further analyzed using SEM, X-ray diffraction, and fluorescence microscopy. Collectively, these results demonstrate the complex behaviors of hnRNPK under different conditions and illustrate the properties of the protein in each material state. Transitions of hnRNPK upon condition changes could potentially affect functions of hnRNPK, playing a significant role in regulation of hnRNPK-involved processes in the cell.

Indexed as

Heterogeneous-Nuclear Ribonucleoprotein KRNA-Binding ProteinsHumansProtein AggregatesScattering, Small AngleTemperatureX-Ray DiffractionHeterogeneous-Nuclear Ribonucleoprotein KHNRNPK protein, humanProtein AggregatesRNA-Binding Proteinsaggregateenvironmental factorshnRNPK proteinhydrogelmaterial state transitionsmonomerphase separationprotein characteristics

Identifiers

PMID39941124
PMCPMC11818384

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.