Evidence map›Paper›PMID 42093151›Full record

ArticleBiophysical journal2026

Subdomains of endophilin can drive membrane remodeling and facilitate controlled membrane scission.

Jeriann R Beiter, Feng-Ching Tsai, Patricia Bassereau, Gregory A Voth

Abstract read
In one paragraph

Article in Biophysical journal, 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

5 · Who and what money

Authors and funding

4 authors.

Jeriann R BeiterDepartment of Chemistry, Chicago Center for Theoretical Chemistry, Institute for Biophysical Dynamics, and James Franck Institute, the University of Chicago, Chicago, IL, USA.
Feng-Ching TsaiInstitut Curie, Université PSL, Sorbonne Université, CNRS UMR168, Physique des Cellules et Cancer, Paris, France.
Patricia BassereauInstitut Curie, Université PSL, Sorbonne Université, CNRS UMR168, Physique des Cellules et Cancer, Paris, France.
Gregory A VothDepartment of Chemistry, Chicago Center for Theoretical Chemistry, Institute for Biophysical Dynamics, and James Franck Institute, the University of Chicago, Chicago, IL, USA. Electronic address: gavoth@uchicago.edu.

Funding

Multiscale Simulation of Key Biomolecular Processes in the CellR35GM158238 · NIGMS · UNIVERSITY OF CHICAGO · PI VOTH, GREGORY A. · 2025 to 2025
$2.0M
NIGMS NIH HHS R35 GM158238
6 · The paper itself

Abstract

The NBAR-domain-containing protein endophilin, a major player in many endocytic pathways, has offered considerable insight into Bin/amphiphysin/Rvs (BAR)-domain-driven membrane remodeling. However, understanding how the different subdomains of endophilin interact and how they sense and generate negative Gaussian curvature remains an unanswered question, with significant implications for the mechanisms and regulation of unconventional endocytic pathways. Using coarse-grained molecular dynamics simulation, we demonstrate the synergistic remodeling capabilities of the NBAR remodeling unit, as well as its ability to sort to and generate membrane regions with negative Gaussian curvature. We find that the assembly of NBAR scaffolds at regions of negative Gaussian curvature facilitates membrane hemifission in dynamic bud formation. These insights provide an additional role for endophilin scaffolds in endocytosis and emphasize the importance of developing new ways to study negative Gaussian curvature.

Indexed as

AcyltransferasesAdaptor Proteins, Signal TransducingCell MembraneEndocytosisMolecular Dynamics SimulationProtein Domains2-acylglycerophosphate acyltransferaseAcyltransferasesAdaptor Proteins, Signal Transducing

Identifiers

PMID42093151
PMCPMC13215578

What Socratic holds

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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 Socratic graph.