Viral capsid-membrane interactions propel non-brownian movements of non-enveloped reoviruses during entry

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 is consistent with a multistep entry mechanism in which initial capsid-membrane contact triggers release of the membrane-active μ1N peptide. Together, our data and simulations support a model in which membrane-inserted μ1N may accumulate locally to create retention sites that promote further virus adsorption and progressively restrict 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.

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Publication Details

Journal
PNAS Nexus
Published
2026-10-09
DOI
https://doi.org/10.1093/pnasnexus/pgag350
Primary Topic
Lipid Membrane Structure and Behavior
Type
article
Field-Weighted Citation Impact
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article

Viral capsid-membrane interactions propel non-brownian movements of non-enveloped reoviruses during entry

Steven M. Abel, Pranav Danthi, Mengchi Jiao, Anthony J. Snyder et al.
PNAS Nexus
Lipid Membrane Structure and Behavior
article

Viral capsid-membrane interactions propel non-brownian movements of non-enveloped reoviruses during entry

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

Abstract

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 is consistent with a multistep entry mechanism in which initial capsid-membrane contact triggers release of the membrane-active μ1N peptide. Together, our data and simulations support a model in which membrane-inserted μ1N may accumulate locally to create retention sites that promote further virus adsorption and progressively restrict 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.

PNAS Nexus
Washington University in St. Louis (US), Indiana University Bloomington (US), University of Tennessee at Knoxville (US)
Openalex Percentile: Top 23%
Lipid Membrane Structure and Behavior
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Viral capsid-membrane interactions propel non-brownian movements of non-enveloped reoviruses during entry — Steven M. Abel, Pranav Danthi, et al. · PNAS Nexus (2026) | TGRS Research Map | TGRS