Detailed Information on Publication Record
2012
Intracellular Release of Endocytosed Nanoparticles Upon a Change of Ligand-Receptor Interaction
VÁCHA, Robert, Francisco J. MARTINEZ-VERACOECHEA and Daan FRENKELBasic information
Original name
Intracellular Release of Endocytosed Nanoparticles Upon a Change of Ligand-Receptor Interaction
Authors
VÁCHA, Robert (203 Czech Republic, guarantor, belonging to the institution), Francisco J. MARTINEZ-VERACOECHEA (826 United Kingdom of Great Britain and Northern Ireland) and Daan FRENKEL (826 United Kingdom of Great Britain and Northern Ireland)
Edition
ACS Nano, WASHINGTON, American Chemical Society, 2012, 1936-0851
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10403 Physical chemistry
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 12.062
RIV identification code
RIV/00216224:14740/12:00064625
Organization unit
Central European Institute of Technology
UT WoS
000312563600020
Keywords in English
cytosol release; late endosome; ligand-receptor interaction; phospholipid membrane; nanoparticle shape; molecular dynamics
Tags
International impact, Reviewed
Změněno: 3/4/2013 07:49, Olga Křížová
Abstract
V originále
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.
Links
ED1.1.00/02.0068, research and development project |
| ||
286154, interní kód MU |
|