Evidence map›Paper›PMID 28180305›Full record

ArticleNucleic acids research2017

Disentangling polydispersity in the PCNA-p15PAF complex, a disordered, transient and multivalent macromolecular assembly.

Tiago N Cordeiro, Po-Chia Chen, Alfredo De Biasio, Nathalie Sibille, Francisco J Blanco, Jochen S Hub, Ramon Crehuet, Pau Bernadó

Open access · goldAbstract readValidation Study
In one paragraph

Article in Nucleic acids research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.1field-weighted citation impact, top 8% of its field
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

13 citing papers in PubMed, 41 citations in OpenAlex.

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  4. Small-Angle X-Ray Scattering for Macromolecular Complexes.Advances in experimental medicine and biology · 2024
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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 at 5 institutions in 4 countries.

Tiago N CordeiroCentre de Biochimie Structurale, INSERM-U1054, CNRS UMR-5048, Université de Montpellier, Montpellier, France.
Po-Chia ChenInstitute for Microbiology and Genetics, Georg-August-University Göttingen, Göttingen, Lower Saxony, Germany.
Alfredo De BiasioElettra-Sincrotrone Trieste S.C.p.A., Trieste, Italy.
Nathalie SibilleCentre de Biochimie Structurale, INSERM-U1054, CNRS UMR-5048, Université de Montpellier, Montpellier, France.
Francisco J BlancoCIC-bioGUNE, Derio, Spain.
Jochen S HubInstitute for Microbiology and Genetics, Georg-August-University Göttingen, Göttingen, Lower Saxony, Germany.
Ramon CrehuetInstitute of Advanced Chemistry of Catalonia, CSIC, Barcelona 08034, Spain.
Pau BernadóCentre de Biochimie Structurale, INSERM-U1054, CNRS UMR-5048, Université de Montpellier, Montpellier, France.
Centre National de la Recherche Scientifique · FRUniversity of Göttingen · DEElettra-Sincrotrone Trieste S.C.p.A. · ITIkerbasque · ESInstitute of Advanced Chemistry of Catalonia · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The intrinsically disordered p15PAF regulates DNA replication and repair when interacting with the Proliferating Cell Nuclear Antigen (PCNA) sliding clamp. As many interactions between disordered proteins and globular partners involved in signaling and regulation, the complex between p15PAF and trimeric PCNA is of low affinity, forming a transient complex that is difficult to characterize at a structural level due to its inherent polydispersity. We have determined the structure, conformational fluctuations, and relative population of the five species that coexist in solution by combining small-angle X-ray scattering (SAXS) with molecular modelling. By using explicit ensemble descriptions for the individual species, built using integrative approaches and molecular dynamics (MD) simulations, we collectively interpreted multiple SAXS profiles as population-weighted thermodynamic mixtures. The analysis demonstrates that the N-terminus of p15PAF penetrates the PCNA ring and emerges on the back face. This observation substantiates the role of p15PAF as a drag regulating PCNA processivity during DNA repair. Our study reveals the power of ensemble-based approaches to decode structural, dynamic, and thermodynamic information from SAXS data. This strategy paves the way for deciphering the structural bases of flexible, transient and multivalent macromolecular assemblies involved in pivotal biological processes.

Indexed as

Carrier ProteinsDNA-Binding ProteinsHumansIntrinsically Disordered ProteinsMolecular Dynamics SimulationMultiprotein ComplexesNuclear Magnetic Resonance, BiomolecularProliferating Cell Nuclear AntigenProtein Structure, QuaternaryRecombinant ProteinsScattering, Small AngleX-Ray DiffractionCarrier ProteinsDNA-Binding ProteinsIntrinsically Disordered ProteinsMultiprotein ComplexesPCLAF protein, humanProliferating Cell Nuclear AntigenRecombinant Proteins

Identifiers

PMID28180305
PMCPMC5388412
OpenAlexW2559964224

What OpenQuestion 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 OpenQuestion graph.