Evidence map›Paper›PMID 40574330›Full record

ArticleBiophysical journal2025

Unraveling viral protein-host membrane interaction for dengue and Zika.

Natalia Philipp, Guadalupe S Costa Navarro, Luana de Borba, Andrea V Gamarnik, Laura C Estrada

Abstract read
In one paragraph

Article in Biophysical journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

5 authors.

Natalia PhilippUniversidad de Buenos Aires, Facultad de Ciencias Exactas y Naturales, Departamento de Física, Buenos Aires, Argentina; CONICET - Universidad de Buenos Aires, Instituto de Física de Buenos Aires (IFIBA), Buenos Aires, Argentina.
Guadalupe S Costa NavarroFundación Instituto Leloir - Instituto de Investigaciones Bioquímicas de Buenos Aires (IIBBA-CONICET), Buenos Aires, Argentina.
Luana de BorbaFundación Instituto Leloir - Instituto de Investigaciones Bioquímicas de Buenos Aires (IIBBA-CONICET), Buenos Aires, Argentina.
Andrea V GamarnikFundación Instituto Leloir - Instituto de Investigaciones Bioquímicas de Buenos Aires (IIBBA-CONICET), Buenos Aires, Argentina.
Laura C EstradaUniversidad de Buenos Aires, Facultad de Ciencias Exactas y Naturales, Departamento de Física, Buenos Aires, Argentina; CONICET - Universidad de Buenos Aires, Instituto de Física de Buenos Aires (IFIBA), Buenos Aires, Argentina. Electronic address: lestrada@df.uba.ar.

Funding

Viral Immunity and VAccination (VIVA) Human Immunology Project Consortium (HIPC)U19AI168631 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Viviana A Simon · 2022 to 2026
$14.4M
MECHANISMS OF DENGUE VIRUS GENOME ENCAPSIDATION AND UNCOATINGR01AI095175 · NIAID · FUNDACION INSTITUTO LELOIR · PI GAMARNIK, ANDREA · 2011 to 2020
$1.0M
NIAID NIH HHS R01 AI095175NIAID NIH HHS U19 AI168631
6 · The paper itself

Abstract

Mosquito-borne flaviviruses, including dengue virus (DENV) and Zika virus (ZIKV), constitute a significant and escalating public health threat. Elucidating the mechanisms by which these flaviviruses subvert cellular processes through viral protein-host cell interactions provides critical insights into their replication and pathogenicity. Here, we present an analysis based on anisotropy calculation across pixels in raster images to investigate differential protein interactions during nucleocytoplasmic shuttling. This methodology highlights regions of high and low anisotropy, suggesting differential protein-membrane interactions. Employing numerical simulations and confocal raster images, we use this method to investigate capsid (C) protein-host cell membrane interactions for DENV serotype 2 (DENV2) and ZIKV-transfected cells during C-protein nucleocytoplasmic shuttling. By 2D pair correlation analysis on infected cells, we demonstrated that the DENV2 C-protein exhibits a pronounced interaction with the host cell's nuclear membrane. Furthermore, we identified a differential localization of C-protein for these viruses in the host cell. These findings highlight the significance of comparative viral protein-host interaction mapping in deciphering pathogenic mechanisms, particularly when combined with in vivo models. Given that dengue and Zika are two of the most significant human viral infections transmitted by arthropods, a thorough understanding of viral protein dynamics is imperative for developing novel antiviral strategies.

Indexed as

Capsid ProteinsCell MembraneDengueDengue VirusHost-Pathogen InteractionsViral ProteinsZika VirusAnimalsHumansNuclear EnvelopeCapsid ProteinsViral Proteins

Identifiers

PMID40574330
PMCPMC12414675

What OpenQuestion holds

Textmetadata
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.