Evidence map›Paper›PMID 40197673›Full record

ArticleChemistry (Weinheim an der Bergstrasse, Germany)2025

Chemical Evolution of Early Macromolecules: From Prebiotic Oligopeptides to Self-Organizing Biosystems via Amyloid Formation.

Fruzsina Bencs, Nóra Taricska, Zsolt Dürvanger, Dániel Horváth, Zsolt Fazekas, Vince Grolmusz, Viktor Farkas, András Perczel

Abstract read
In one paragraph

Article in Chemistry (Weinheim an der Bergstrasse, Germany), 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. 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

8 authors.

Fruzsina BencsELTE Hevesy György PhD School of Chemistry, ELTE Eötvös Loránd University, Pázmány Péter sétány 1/A, Budapest, H-1117, Hungary.ORCID https://orcid.org/0009-0003-9246-2228
Nóra TaricskaLaboratory of Structural Chemistry and Biology, Institute of Chemistry, ELTE Eötvös Loránd University, Pázmány Péter sétány 1/A, Budapest, H-1117, Hungary.ORCID https://orcid.org/0000-0002-9721-953X
Zsolt DürvangerLaboratory of Structural Chemistry and Biology, Institute of Chemistry, ELTE Eötvös Loránd University, Pázmány Péter sétány 1/A, Budapest, H-1117, Hungary.ORCID https://orcid.org/0000-0002-2652-4916
Dániel HorváthLaboratory of Structural Chemistry and Biology, Institute of Chemistry, ELTE Eötvös Loránd University, Pázmány Péter sétány 1/A, Budapest, H-1117, Hungary.ORCID https://orcid.org/0000-0001-8239-3933
Zsolt FazekasELTE Hevesy György PhD School of Chemistry, ELTE Eötvös Loránd University, Pázmány Péter sétány 1/A, Budapest, H-1117, Hungary.ORCID https://orcid.org/0000-0001-5007-4807
Vince GrolmuszGroup of Protein Information Technology, Department of Computer Science, ELTE Eötvös Loránd University, Pázmány Péter sétány 1/C, Budapest, H-1117, Hungary.ORCID https://orcid.org/0000-0001-9456-8876
Viktor FarkasLaboratory of Structural Chemistry and Biology, Institute of Chemistry, ELTE Eötvös Loránd University, Pázmány Péter sétány 1/A, Budapest, H-1117, Hungary.ORCID https://orcid.org/0000-0002-8815-2783
András PerczelLaboratory of Structural Chemistry and Biology, Institute of Chemistry, ELTE Eötvös Loránd University, Pázmány Péter sétány 1/A, Budapest, H-1117, Hungary.ORCID https://orcid.org/0000-0003-1252-6416

Funding

European Regional Development Fund VEKOP-2.3.3-15-2017-00018European Union's Recovery and Resilience Instrument RRF-2.3.1-21-2022-00015Nemzeti Kutatási, Fejlesztési és Innovaciós Alap 2018-1.2.1-NKP-2018-00005
6 · The paper itself

Abstract

Short amyloidogenic oligopeptides (APRs) are proposed as early macromolecules capable of forming solvent-separated nanosystems under prebiotic conditions. This study provides experimental evidence that APRs, such as the aggregation-prone oligopeptide A (APR-A), can undergo mutational transitions to form distinct variants and convert to APR-B, either amyloid-like or water-soluble and non-aggregating. These transitions occur along a spectrum from strongly amyloidogenic (pro-amyloid) to weakly amyloidogenic (anti-amyloid), with the mutation sequence order playing a key role in determining their physicochemical properties. The pro-amyloid pathway facilitates heterogeneous phase separation, leading to amyloid-crystal formation with multiple polymorphs, including the first class 3 amyloid topology. By mapping these transitions, we demonstrate the potential co-evolution of water-soluble miniproteins and insoluble amyloids, both of which could have been pivotal in early bio-nanosystem formation. These insights into amyloid modulation provide a crucial step toward understanding amyloid control mechanisms.

Indexed as

AmyloidMacromolecular SubstancesOligopeptidesEvolution, ChemicalWaterAmyloidMacromolecular SubstancesOligopeptidesWaterAFM of amyloidogenic oligopeptidesaggregation‐prone regionsamyloid X‐ray structureECD‐ and FTIR‐spectroscopymolecular evolution

Identifiers

PMID40197673
PMCPMC12099175

What Socratic holds

Textmetadata
LicenceCC BY-NC
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.