Evidence map›Paper›PMID 40329536›Full record

ArticleBiophysical journal2025

Effect of RNA on the supramolecular architecture of α-synuclein fibrils.

Antonia Intze, Maria Eleonora Temperini, Jakob Rupert, Raffaella Polito, Alexander Veber, Ljiljana Puskar, Ulrich Schade, Michele Ortolani, Elsa Zacco, Gian Gaetano Tartaglia and 1 more

Abstract read
In one paragraph

Article in Biophysical journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Antonia IntzeCenter for Life Nano- & Neuro-science, Istituto Italiano di Tecnologia (IIT), Rome, Italy; Department of Biochemical Sciences "Alessandro Rossi Fanelli", Sapienza University of Rome, Rome, Italy; Department of Physics, Sapienza University of Rome, Rome, Italy. Electronic address: antonia.intze@uniroma1.it.
Maria Eleonora TemperiniCenter for Life Nano- & Neuro-science, Istituto Italiano di Tecnologia (IIT), Rome, Italy; Department of Physics, Sapienza University of Rome, Rome, Italy.
Jakob RupertDepartment of Biology and Biotechnologies "Charles Darwin", Sapienza University of Rome, Rome, Italy; Centre for Human Technologies (CHT), Istituto Italiano di Tecnologia (IIT), Genova, Italy; Molecular Neuroscience, German Center for Neurodegenerative Diseases (DZNE), Bonn, Germany.
Raffaella PolitoDepartment of Physics, Sapienza University of Rome, Rome, Italy; Institute for Photonics and Nanotechnologies IFN-CNR, Rome, Italy.
Alexander VeberInstitute for Electronic Structure Dynamics, Helmholtz-Zentrum Berlin für Materialien und Energie GmbH, Berlin, Germany; Department of Chemistry, Humboldt-Universität zu Berlin, Berlin, Germany.
Ljiljana PuskarInstitute for Electronic Structure Dynamics, Helmholtz-Zentrum Berlin für Materialien und Energie GmbH, Berlin, Germany.
Ulrich SchadeInstitute for Electronic Structure Dynamics, Helmholtz-Zentrum Berlin für Materialien und Energie GmbH, Berlin, Germany.
Michele OrtolaniDepartment of Physics, Sapienza University of Rome, Rome, Italy.
Elsa ZaccoCentre for Human Technologies (CHT), Istituto Italiano di Tecnologia (IIT), Genova, Italy.
Gian Gaetano TartagliaCentre for Human Technologies (CHT), Istituto Italiano di Tecnologia (IIT), Genova, Italy; Catalan Institution for Research and Advanced Studies, ICREA, Barcelona, Spain.
Valeria GilibertiCenter for Life Nano- & Neuro-science, Istituto Italiano di Tecnologia (IIT), Rome, Italy. Electronic address: valeria.giliberti@iit.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Structural changes associated with protein aggregation are challenging to study, requiring the combination of experimental techniques providing insights at the molecular level across diverse scales, ranging from nanometers to microns. Understanding these changes is even more complex when aggregation occurs in the presence of molecular cofactors such as nucleic acids and when the resulting aggregates are highly polymorphic. Infrared (IR) spectroscopy is a powerful tool for studying protein aggregates since it combines the label-free sensitivity to the cross-β architecture, an inherent feature of protein supramolecular aggregates, with the possibility to reach nanoscale sensitivity by leveraging atomic force microscopy (AFM)-assisted detection. Here, we present a combined approach that detects IR spectral markers of aggregation using various IR spectroscopy techniques, covering micro-to-nanoscale ranges, to study the effect of RNA on the supramolecular architecture of α-synuclein amyloid aggregates. We show a clear impact of RNA consistent with enhanced intermolecular forces, likely via a stronger hydrogen-bonded network stabilizing the cross-β architecture. AFM-assisted IR spectroscopy was crucial to assess that the more ordered the aggregates are, the stronger the structural impact of RNA. In addition, an RNA-induced reduction of the degree of polymorphism within the aggregate population is obtained.

Indexed as

alpha-SynucleinAmyloidRNAHumansMicroscopy, Atomic ForceProtein AggregatesSpectrophotometry, Infraredalpha-SynucleinAmyloidProtein AggregatesRNA

Identifiers

PMID40329536
PMCPMC12256921

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.