Evidence map›Paper›PMID 39875596›Full record

ArticleCommunications chemistry2025

Biophysical and spectroscopical insights into structural modulation of species in the aggregation pathway of superoxide dismutase 1.

Vijay Raj Tomar, Shilpa Sharma, Soumik Siddhanta, Shashank Deep

Abstract read
In one paragraph

Article in Communications chemistry, 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

4 authors.

Vijay Raj Tomar *Department of Chemistry, Indian Institute of Technology Delhi, New Delhi, India.
Shilpa Sharma *Department of Chemistry, Indian Institute of Technology Delhi, New Delhi, India.
Soumik SiddhantaDepartment of Chemistry, Indian Institute of Technology Delhi, New Delhi, India. soumik@iitd.ac.in.ORCID http://orcid.org/0000-0002-1383-6224
Shashank DeepDepartment of Chemistry, Indian Institute of Technology Delhi, New Delhi, India. sdeep@chemistry.iitd.ac.in.ORCID http://orcid.org/0000-0002-4908-8205

Funding

DST | Science and Engineering Research Board (SERB) CRG/2020/002091
6 · The paper itself

Abstract

Superoxide dismutase 1 (SOD1) aggregation is implicated in the development of Amyotrophic Lateral Sclerosis (ALS). Despite knowledge of the role of SOD1 aggregation, the mechanistic understanding remains elusive. Our investigation aimed to unravel the complex steps involved in SOD1 aggregation associated with ALS. Therefore, we probed the aggregation using ThT fluorescence, size-exclusion chromatography, and surface-enhanced Raman spectroscopy (SERS). The removal of metal ions and disulfide bonds resulted in the dimers rapidly first converting to an extended monomers then coming together slowly to form non-native dimers. The rapid onset of oligomerization happens above critical non-native dimer concentration. Structural features of oligomer was obtained through SERS. The kinetic data supported a fragmentation-dominant mechanism for the fibril formation. Quercetin acts as inhibitor by delaying the formation of non-native dimer and soluble oligomers by decreasing the elongation rate. Thus, results provide significant insights into the critical steps in oligomer formation and their structure.

Identifiers

PMID39875596
PMCPMC11775178

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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.