Evidence map›Paper›PMID 38464093›Full record

ArticlebioRxiv : the preprint server for biology2024

Phase Separation and Aggregation of α-Synuclein Diverge at Different Salt Conditions.

Rebecca Sternke-Hoffmann, Xun Sun, Andreas Menzel, Miriam Dos Santos Pinto, Urtė Venclovaitė, Michael Wördehoff, Wolfgang Hoyer, Wenwei Zheng, Jinghui Luo

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 3 countries.

Rebecca Sternke-HoffmannDepartment of Biology and Chemistry, Paul Scherrer Institute, Forschungsstrasse 111, 5232 Villigen PSI, Switzerland.ORCID 0000-0002-1662-8244
Xun SunDepartment of Biology and Chemistry, Paul Scherrer Institute, Forschungsstrasse 111, 5232 Villigen PSI, Switzerland.
Andreas MenzelPhoton Science Division, Paul Scherrer Institute, Forschungsstrasse 111, 5232 Villigen PSI, Switzerland.
Miriam Dos Santos PintoDepartment of Biology and Chemistry, Paul Scherrer Institute, Forschungsstrasse 111, 5232 Villigen PSI, Switzerland.
Urtė VenclovaitėDepartment of Biology and Chemistry, Paul Scherrer Institute, Forschungsstrasse 111, 5232 Villigen PSI, Switzerland.
Michael WördehoffInstitut für Physikalische Biologie, Heinrich-Heine University Düsseldorf, 40225 Düsseldorf, Germany.
Wolfgang HoyerInstitut für Physikalische Biologie, Heinrich-Heine University Düsseldorf, 40225 Düsseldorf, Germany.
Wenwei ZhengCollege of Integrative Sciences and Arts, Arizona State University, Mesa, AZ, 85212, United States.ORCID 0000-0002-9603-009X
Jinghui LuoDepartment of Biology and Chemistry, Paul Scherrer Institute, Forschungsstrasse 111, 5232 Villigen PSI, Switzerland.
Paul Scherrer Institute · CHHeinrich Heine University Düsseldorf · DEArizona State University · US

Funding

Decoding the mechanism of disordered protein interactionsR35GM146814 · NIGMS · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI Wenwei Zheng · 2022 to 2026
$1.8M
NIGMS NIH HHS R35 GM146814
6 · The paper itself

Abstract

The coacervation and structural rearrangement of the protein alpha-synuclein (αSyn) into cytotoxic oligomers and amyloid fibrils are considered pathological hallmarks of Parkinson's disease. While aggregation is recognized as the key element of amyloid diseases, liquid-liquid phase separation (LLPS) and its interplay with aggregation have gained increasing interest. Previous work showed that factors promoting or inhibiting amyloid formation have similar effects on phase separation. Here, we provide a detailed scanning of a wide range of parameters including protein, salt and crowding concentrations at multiple pH values, revealing different salt dependencies of aggregation and phase separation. The influence of salt on aggregation under crowded conditions follows a non-monotonic pattern, showing increased effects at medium salt concentrations. This behavior can be elucidated through a combination of electrostatic screening and salting-out effects on the intramolecular interactions between the N-terminal and C-terminal regions of αSyn. By contrast, we find a monotonic salt dependence of phase separation due to the intermolecular interaction. Furthermore, we observe the time evolution of the two distinct assembly states, with macroscopic fibrillar-like bundles initially forming at medium salt concentration but subsequently converting into droplets after prolonged incubation. The droplet state is therefore capable of inhibiting aggregation or even dissolving the aggregates through a variety of heterotypic interactions, thus preventing αSyn from its dynamically arrested state.

Indexed as

AggregationBiomolecular CondensatesIntrinsically Disordered ProteinsLiquid-Liquid Phase SeparationMolecular Dynamics

Identifiers

PMID38464093
PMCPMC10925286
OpenAlexW4392344106

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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 OpenQuestion graph.