Intracellular release of endocytosed nanoparticles upon a change of ligand-receptor interaction
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
23148579
DOI
10.1021/nn303508c
Knihovny.cz E-zdroje
- MeSH
- buněčná membrána metabolismus MeSH
- endocytóza * MeSH
- fosfolipidy metabolismus MeSH
- hydrofobní a hydrofilní interakce MeSH
- intracelulární prostor metabolismus MeSH
- koncentrace vodíkových iontů MeSH
- ligandy MeSH
- molekulární konformace MeSH
- nanočástice * MeSH
- rozpouštědla chemie MeSH
- simulace molekulární dynamiky * MeSH
- termodynamika MeSH
- vazba proteinů MeSH
- velikost částic MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- fosfolipidy MeSH
- ligandy MeSH
- rozpouštědla MeSH
During passive endocytosis, nanosized particles are initially encapsulated by a membrane separating it from the cytosol. Yet, in many applications the nanoparticles need to be in direct contact with the cytosol in order to be active. We report a simulation study that elucidates the physical mechanisms by which such nanoparticles can shed their bilayer coating. We find that nanoparticle release can be readily achieved by a pH-induced lowering of the attraction between nanoparticle and membrane only if the nanoparticle is either very small or nonspherical. Interestingly, we find that in the case of large spherical nanoparticles, the reduction of attraction needs to be accompanied by exerting an additional tension on the membrane (e.g., via nanoparticle expansion) to achieve release. We expect these findings will contribute to the rational design of drug delivery strategies via nanoparticles.
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