Evidence map›Paper›PMID 40166240›Full record

ArticlebioRxiv : the preprint server for biology2025

Single VLP lipid-mixing measurements confirm off-pathway state in dengue virus fusion mechanism.

Tasnim K Anika, Fiona Campbell, Bianca Linden, Connor J Criswell, Miranda Kimm, Priscilla Li-Ning Yang, Robert J Rawle

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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

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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

5 · Who and what money

Authors and funding

7 authors.

Tasnim K AnikaDepartment of Chemistry, Williams College, Williamstown, MA, 01267, USA.
Fiona CampbellDepartment of Chemistry, Williams College, Williamstown, MA, 01267, USA.
Bianca LindenDepartment of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Connor J CriswellDepartment of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Miranda KimmDepartment of Chemistry, Williams College, Williamstown, MA, 01267, USA.
Priscilla Li-Ning YangDepartment of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Robert J RawleDepartment of Chemistry, Williams College, Williamstown, MA, 01267, USA.ORCID 0000-0003-4958-4919

Funding

Validating the Flavivirus Envelope Protein as an Antiviral TargetR01AI146152 · NIAID · STANFORD UNIVERSITY · PI GRAY, NATHANAEL SCHIANDER, YANG, PRISCILLA LI-NING · 2020 to 2024
$4.6M
Investigation of the biophysical mechanisms and membrane determinants ofrespirovirus binding and fusion using artificial lipid membranes and isolatedphysiological membranes as targetsR15AI171754 · NIAID · WILLIAMS COLLEGE · PI Robert J. Rawle · 2022 to 2026
$879k
OneView 4kX4k sCMOS camera for transmission electron microscopy applicationsS10OD028536 · OD · STANFORD UNIVERSITY · PI MULHOLLAND, JONATHAN W · 2020 to 2020
$195k
NIAID NIH HHS R01 AI146152NIAID NIH HHS R15 AI171754NIH HHS S10 OD028536
6 · The paper itself

Abstract

Dengue virus (DENV) is the causative agent of dengue fever and exerts a substantial healthcare burden worldwide. Like other flaviviruses, DENV must undergo membrane fusion with the host cell in order to initiate infection. This membrane fusion occurs following acidification during endocytosis and is pH dependent. Here, we interrogate whether the mechanism of DENV fusion contains an off-pathway state, such has been reported previously for two other flaviviruses - Zika virus and West Nile virus. To do this, we utilize single particle lipid mixing measurements of DENV virus-like particles (VLPs) to tethered liposomes, together with computational modeling inspired by chemical kinetics. By observing and then modeling the pH dependence of single VLP fusion kinetics, we provide evidence that the DENV fusion mechanism must contain an off-pathway state. Measuring the proportion of VLPs undergoing hemi-fusion over time, we also demonstrate that the off-pathway state appears to be slowly reversible over tens of minutes, at least for some virions. Additionally, we find that late endosomal anionic lipids do not appear to influence the off-pathway mechanism to any great extent. In conjunction with the prior reports on Zika virus and West Nile virus, this work indicates that an off-pathway fusion state may be a feature of flavivirus fusion more broadly. We also note that the platform and mechanistic model described in this study may be useful in elucidating the mechanism of action of small molecule inhibitors of flavivirus fusion developed by our group and others.

Identifiers

PMID40166240
PMCPMC11957162

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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.