ArticleThe Journal of membrane biology2026
Membrane Remodeling Activity of Dengue Virus NS4A and NS1 Proteins: A Computational Perspective.
Article in The Journal of membrane biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Dengue virus (DENV) non-structural protein NS4A and NS1 are crucial for viral replication and have the ability to cause extensive remodeling of the host cell membrane. Here, a computational strategy has been used to study the structural and functional aspects of NS4A and NS1 in membrane interaction and remodeling. By employing multiscale all atom and coarse grained molecular dynamics simulations, we investigated the conformational dynamics of NS4A and NS1 and their interactions with model lipid bilayers. Our results establish that NS4A inserts preferentially into membranes in its native state as an integral membrane protein and causes curvature aided by its oligomerization event, which is in agreement with its proposed function in replication complex formation. NS1 has stable lipid-binding domains that can anchor and induce membrane curvature or stabilize remodelled membrane structures and perform its function as a peripherally bound membrane protein. These findings give molecular-level insights into the mechanism of how DENV hijacks host membranes for replication and identify potential targets for antiviral interventions. This study also plays an important role in updating our knowledge of flaviviral manipulation of membranes.
Indexed as
Identifiers
41642338What OpenQuestion holds
Registered trials
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.