Intracellular Release of Endocytosed Nanoparticles Upon a Change of Ligand-Receptor Interaction

被引:52
作者
Vacha, Robert [1 ,2 ]
Martinez-Veracoechea, Francisco J. [3 ]
Frenkel, Daan [3 ]
机构
[1] Masaryk Univ, Fac Sci, Natl Ctr Biomol Res, Brno 62500, Czech Republic
[2] Masaryk Univ, CEITEC Cent European Inst Technol, Brno 62500, Czech Republic
[3] Univ Cambridge, Dept Chem, Cambridge CB2 1EW, England
关键词
cytosol release; late endosome; ligand-receptor interaction; phospholipid membrane; nanoparticle shape; molecular dynamics; GIANT VESICLES; TENSION; PORES; ELASTICITY; PROTEINS; ENERGY;
D O I
10.1021/nn303508c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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. © 2012 American Chemical Society.
引用
收藏
页码:10598 / 10605
页数:8
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