Evidence map›Paper›PMID 36050301›Full record

ArticleNature communications2022

Percolation transition prescribes protein size-specific barrier to passive transport through the nuclear pore complex.

David Winogradoff, Han-Yi Chou, Christopher Maffeo, Aleksei Aksimentiev

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.3field-weighted citation impact, top 6% 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

21 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Article
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  5. Integrative mapping reveals molecular features underlying the mechanism of nucleocytoplasmic transport.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  6. Review
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  11. Article
  12. Article
  13. Article
  14. HIV-1 capsid shape, orientation, and entropic elasticity regulate translocation into the nuclear pore complex.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  15. Review
  16. Phase separation of intrinsically disordered FG-Nups is driven by highly dynamic FG motifs.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
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  20. 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 at 1 institution in 1 country.

David Winogradoff *Department of Physics, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, USA.ORCID 0000-0002-1982-2093
Han-Yi Chou *Department of Physics, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, USA.
Christopher MaffeoDepartment of Physics, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, USA.ORCID 0000-0001-9927-1502
Aleksei AksimentievDepartment of Physics, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, USA. aksiment@illinois.edu.ORCID 0000-0002-6042-8442
University of Illinois Urbana-Champaign · US

Funding

WHOLE CELL SIMULATIONP41GM104601 · NIGMS · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI TAJKHORSHID, EMAD · 2012 to 2021
$19.0M
Multi-resolution Approaches to Modeling the 3D Structure, Delivery, and Replication of Viral GenomesR01GM137015 · NIGMS · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI AKSIMENTIEV, ALEKSEI · 2020 to 2023
$1.2M
NIGMS NIH HHS P41 GM104601NIGMS NIH HHS R01 GM137015
6 · The paper itself

Abstract

Nuclear pore complexes (NPCs) control biomolecular transport in and out of the nucleus. Disordered nucleoporins in the complex's pore form a permeation barrier, preventing unassisted transport of large biomolecules. Here, we combine coarse-grained simulations of experimentally derived NPC structures with a theoretical model to determine the microscopic mechanism of passive transport. Brute-force simulations of protein transport reveal telegraph-like behavior, where prolonged diffusion on one side of the NPC is interrupted by rapid crossings to the other. We rationalize this behavior using a theoretical model that reproduces the energetics and kinetics of permeation solely from statistics of transient voids within the disordered mesh. As the protein size increases, the mesh transforms from a soft to a hard barrier, enabling orders-of-magnitude reduction in permeation rate for proteins beyond the percolation size threshold. Our model enables exploration of alternative NPC architectures and sets the stage for uncovering molecular mechanisms of facilitated nuclear transport.

Indexed as

Nuclear PoreNuclear Pore Complex ProteinsActive Transport, Cell NucleusDiffusionKineticsNuclear Pore Complex Proteins

Identifiers

PMID36050301
PMCPMC9437005
OpenAlexW4294001680

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.