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Updated: May 8, 2026

In Vitro Polymerization of F-actin on Early Endosomes
Published on: August 28, 2017
Subdomains of endophilin can drive membrane remodeling and facilitate controlled membrane scission
Jeriann R Beiter1, Feng-Ching Tsai2, Patricia Bassereau2
1Department of Chemistry, Chicago Center for Theoretical Chemistry, Institute for Biophysical Dynamics, and James Franck Institute, the University of Chicago, Chicago, IL, USA.
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.
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