Evidence map›Paper›PMID 41648579›Full record

ArticlebioRxiv : the preprint server for biology2026

Viral Capsid-Membrane Interactions Propel Non-Brownian Movements of Non-enveloped Reoviruses during Entry.

Mengchi Jiao, Gregory R Cantrall, Yanqi Yu, Anthony J Snyder, Steven M Abel, Pranav Danthi, Yan Yu

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. 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.

No citing paper in PubMed yet.

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

7 authors.

Mengchi JiaoDepartment of Chemistry, Indiana University, Bloomington, IN 47405-7102.ORCID 0000-0001-5958-0706
Gregory R CantrallDepartment of Chemical and Biomolecular Engineering, University of Tennessee, Knoxville, TN 37996.ORCID 0000-0003-4138-4971
Yanqi YuDepartment of Chemistry, Indiana University, Bloomington, IN 47405-7102.ORCID 0000-0002-6969-3752
Anthony J SnyderDepartment of Biology, Indiana University, Bloomington, IN 47405-7102.ORCID 0000-0002-2551-9461
Steven M AbelDepartment of Chemical and Biomolecular Engineering, University of Tennessee, Knoxville, TN 37996.ORCID 0000-0003-0491-8647
Pranav DanthiDepartment of Biology, Indiana University, Bloomington, IN 47405-7102.ORCID 0000-0001-6199-6022
Yan YuDepartment of Chemistry, Department of Biomedical Engineering, Washington University in St. Louis, St. Louis, MO 63130.ORCID 0000-0001-6496-5045

Funding

Unravelling Mechanisms of Endosomal Signaling with Designer NanomaterialsR35GM124918 · NIGMS · WASHINGTON UNIVERSITY · PI Yan Yu · 2017 to 2026
$3.8M
Real-time single particle analysis of reovirus-membrane interactions that drive infectionR21AI171911 · NIAID · TRUSTEES OF INDIANA UNIVERSITY · PI DANTHI, PRANAV, YU, YAN · 2022 to 2023
$420k
NIAID NIH HHS R21 AI171911NIGMS NIH HHS R35 GM124918
6 · The paper itself

Abstract

Understanding how non-enveloped viruses breach host cell membranes is critical for developing strategies to block viral entry, a key step in infection. Despite extensive study, how viral capsids and host lipid membranes dynamically cooperate during membrane penetration remains poorly defined. Here, using reovirus as a model non-enveloped virus and planar model membranes, we identify previously unrecognized non-Brownian membrane motions of infectious subvirion particles (ISVPs) by single-virus tracking. We then integrate experiments with computational modeling to dissect the stepwise, processive capsid-membrane interactions encoded in these distinct dynamics. We show that ISVP motion transitions from an initial phase of directed translocation to progressively confined diffusion. This behavior reflects a multistep entry mechanism in which initial capsid-membrane contact triggers release of the membrane-active μ1N peptide. As μ1N accumulates within the bilayer, it generates membrane-associated viral retention sites that promote further virus adsorption and increasingly constrain particle mobility. By directly visualizing these motion signatures, we resolve transient and cooperative capsid-membrane interactions that are difficult to capture using conventional biochemical approaches. Together, these findings provide new insight into early membrane penetration events of non-enveloped viruses.

Identifiers

PMID41648579
PMCPMC12871715

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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.