Protein‐Sized Dye‐Loaded Polymer Nanoparticles for Free Particle Diffusion in Cytosol. (11th October 2018)
- Record Type:
- Journal Article
- Title:
- Protein‐Sized Dye‐Loaded Polymer Nanoparticles for Free Particle Diffusion in Cytosol. (11th October 2018)
- Main Title:
- Protein‐Sized Dye‐Loaded Polymer Nanoparticles for Free Particle Diffusion in Cytosol
- Authors:
- Reisch, Andreas
Heimburger, Doriane
Ernst, Pauline
Runser, Anne
Didier, Pascal
Dujardin, Denis
Klymchenko, Andrey S. - Abstract:
- Abstract: How small should nanoparticles be in order to travel freely through the cytosol similar to proteins? Answering this question remains a challenge, because the majority of nanoparticles are relatively large and their size cannot be finely tuned to match that of proteins. Here, poly(methyl methacrylate) copolymers with varied fraction and type of charged groups (carboxylate, sulfonate, and trimethylammonium) are developed, yielding nanoparticles with controlled sizes from 50 to 7 nm through nanoprecipitation. Loading these nanoparticles with a rhodamine dye/bulky counterion pair at 10wt% makes them highly fluorescent. After their coating with polyethylene glycol groups for preventing non‐specific protein binding and microinjection into living cells, the first systematic study of the size effect on diffusion in the cytosol for solid nanoparticles of the same nature is realized. Single‐particle‐tracking data provide evidence for distinct particle sieving in the cytosol, suggesting that only nanoparticles below a critical size of 23 nm exhibit free diffusion and spreading. These findings show the size limitations imposed by intracellular crowding and compartmentalization, which is critical for applications of nanomaterials in the cytosol. The proposed concept of polymer design opens the route to organic nanoparticles of ultrasmall sizes and high loading for bioimaging and drug‐delivery applications. Abstract : What is the ideal size of nanoparticles (NPs) forAbstract: How small should nanoparticles be in order to travel freely through the cytosol similar to proteins? Answering this question remains a challenge, because the majority of nanoparticles are relatively large and their size cannot be finely tuned to match that of proteins. Here, poly(methyl methacrylate) copolymers with varied fraction and type of charged groups (carboxylate, sulfonate, and trimethylammonium) are developed, yielding nanoparticles with controlled sizes from 50 to 7 nm through nanoprecipitation. Loading these nanoparticles with a rhodamine dye/bulky counterion pair at 10wt% makes them highly fluorescent. After their coating with polyethylene glycol groups for preventing non‐specific protein binding and microinjection into living cells, the first systematic study of the size effect on diffusion in the cytosol for solid nanoparticles of the same nature is realized. Single‐particle‐tracking data provide evidence for distinct particle sieving in the cytosol, suggesting that only nanoparticles below a critical size of 23 nm exhibit free diffusion and spreading. These findings show the size limitations imposed by intracellular crowding and compartmentalization, which is critical for applications of nanomaterials in the cytosol. The proposed concept of polymer design opens the route to organic nanoparticles of ultrasmall sizes and high loading for bioimaging and drug‐delivery applications. Abstract : What is the ideal size of nanoparticles (NPs) for intracellular applications? Here, a series of dye‐loaded polymer NPs with sizes from 50 down to 7 nm is synthesized and microinjected into living cells. Single‐particle tracking of these particles suggests that only NPs smaller than a critical size of 23 nm exhibit free diffusion and spreading in the cytosol. … (more)
- Is Part Of:
- Advanced functional materials. Volume 28:Number 48(2018)
- Journal:
- Advanced functional materials
- Issue:
- Volume 28:Number 48(2018)
- Issue Display:
- Volume 28, Issue 48 (2018)
- Year:
- 2018
- Volume:
- 28
- Issue:
- 48
- Issue Sort Value:
- 2018-0028-0048-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2018-10-11
- Subjects:
- diffusion in the cytosol -- fluorescent polymer nanoparticles -- intracellular particle sieving -- single‐particle tracking
Materials -- Periodicals
Chemical vapor deposition -- Periodicals
620.11 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1616-3028 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/adfm.201805157 ↗
- Languages:
- English
- ISSNs:
- 1616-301X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0696.853900
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 11960.xml