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Updated: May 2, 2026

Nanopodia - Thin, Fragile Membrane Projections with Roles in Cell Movement and Intercellular Interactions
Published on: April 3, 2014
Membrane monolayer protrusion mediates a new nanoparticle wrapping pathway
Tongtao Yue1, Xianren Zhang, Fang Huang
1State Key Laboratory of Heavy Oil Processing, Center for Bioengineering and Biotechnology, China University of Petroleum (East China), Qingdao, 266580, China. fhuang@upc.edu.cn.
Nanoparticles (NPs) can enter cells via a novel membrane wrapping pathway, distinct from endocytosis. This process, driven by strong NP-membrane adhesion and low membrane tension, involves membrane monolayer protrusion for NP internalization.
Area of Science:
- Biophysics
- Nanotechnology
- Cell Biology
Background:
- Nanoparticle (NP) interactions with lipid membranes are crucial for biomedical applications and understanding cytotoxicity.
- Conventional cellular uptake mechanisms like endocytosis do not fully explain all NP-membrane interactions.
Purpose of the Study:
- To investigate novel pathways of nanoparticle internalization into lipid membranes.
- To elucidate the mechanisms underlying NP wrapping by membranes.
Main Methods:
- Computer simulations were employed to model NP-lipid membrane interactions.
- Free energy analysis was used to support simulation findings.
Main Results:
- A novel NP wrapping pathway, distinct from endocytosis, was identified.
- This pathway is regulated by membrane monolayer protrusion under conditions of strong NP-membrane adhesion and low membrane tension.
- NP internalization can be facilitated by decreasing membrane tension, breaking membrane symmetry, or applying external force.
Conclusions:
- Nanoparticles can internalize via a unique membrane wrapping mechanism mediated by monolayer protrusion.
- This discovery offers new insights into nanoparticle-cell interactions and potential therapeutic delivery strategies.
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