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Protein corona – from molecular adsorption to physiological complexity
In biological environments, nanoparticles are enshrouded by a layer of biomolecules, predominantly proteins, mediating its subsequent interactions with cells. Detecting this protein corona, understanding its formation with regards to nanoparticle (NP) and protein properties, and elucidating its biol...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4419682/ https://www.ncbi.nlm.nih.gov/pubmed/25977856 http://dx.doi.org/10.3762/bjnano.6.88 |
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author | Treuel, Lennart Docter, Dominic Maskos, Michael Stauber, Roland H |
author_facet | Treuel, Lennart Docter, Dominic Maskos, Michael Stauber, Roland H |
author_sort | Treuel, Lennart |
collection | PubMed |
description | In biological environments, nanoparticles are enshrouded by a layer of biomolecules, predominantly proteins, mediating its subsequent interactions with cells. Detecting this protein corona, understanding its formation with regards to nanoparticle (NP) and protein properties, and elucidating its biological implications were central aims of bio-related nano-research throughout the past years. Here, we discuss the mechanistic parameters that are involved in the protein corona formation and the consequences of this corona formation for both, the particle, and the protein. We review consequences of corona formation for colloidal stability and discuss the role of functional groups and NP surface functionalities in shaping NP–protein interactions. We also elaborate the recent advances demonstrating the strong involvement of Coulomb-type interactions between NPs and charged patches on the protein surface. Moreover, we discuss novel aspects related to the complexity of the protein corona forming under physiological conditions in full serum. Specifically, we address the relation between particle size and corona composition and the latest findings that help to shed light on temporal evolution of the full serum corona for the first time. Finally, we discuss the most recent advances regarding the molecular-scale mechanistic role of the protein corona in cellular uptake of NPs. |
format | Online Article Text |
id | pubmed-4419682 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-44196822015-05-14 Protein corona – from molecular adsorption to physiological complexity Treuel, Lennart Docter, Dominic Maskos, Michael Stauber, Roland H Beilstein J Nanotechnol Review In biological environments, nanoparticles are enshrouded by a layer of biomolecules, predominantly proteins, mediating its subsequent interactions with cells. Detecting this protein corona, understanding its formation with regards to nanoparticle (NP) and protein properties, and elucidating its biological implications were central aims of bio-related nano-research throughout the past years. Here, we discuss the mechanistic parameters that are involved in the protein corona formation and the consequences of this corona formation for both, the particle, and the protein. We review consequences of corona formation for colloidal stability and discuss the role of functional groups and NP surface functionalities in shaping NP–protein interactions. We also elaborate the recent advances demonstrating the strong involvement of Coulomb-type interactions between NPs and charged patches on the protein surface. Moreover, we discuss novel aspects related to the complexity of the protein corona forming under physiological conditions in full serum. Specifically, we address the relation between particle size and corona composition and the latest findings that help to shed light on temporal evolution of the full serum corona for the first time. Finally, we discuss the most recent advances regarding the molecular-scale mechanistic role of the protein corona in cellular uptake of NPs. Beilstein-Institut 2015-03-30 /pmc/articles/PMC4419682/ /pubmed/25977856 http://dx.doi.org/10.3762/bjnano.6.88 Text en Copyright © 2015, Treuel et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjnano/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Nanotechnology terms and conditions: (https://www.beilstein-journals.org/bjnano/terms) |
spellingShingle | Review Treuel, Lennart Docter, Dominic Maskos, Michael Stauber, Roland H Protein corona – from molecular adsorption to physiological complexity |
title | Protein corona – from molecular adsorption to physiological complexity |
title_full | Protein corona – from molecular adsorption to physiological complexity |
title_fullStr | Protein corona – from molecular adsorption to physiological complexity |
title_full_unstemmed | Protein corona – from molecular adsorption to physiological complexity |
title_short | Protein corona – from molecular adsorption to physiological complexity |
title_sort | protein corona – from molecular adsorption to physiological complexity |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4419682/ https://www.ncbi.nlm.nih.gov/pubmed/25977856 http://dx.doi.org/10.3762/bjnano.6.88 |
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