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Comparison of the effects of dendrimer, micelle and silver nanoparticles on phospholipase A2 structure

[Display omitted] •'Hard' and 'soft' nanoparticles differently affected phospholipase A2.•'Soft' nanoparticles formed aggregates/micelles with protein.•'Hard' nanoparticle had bimolecular interaction with protein. The interaction of nanoparticles (NP) with pro...

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Bibliographic Details
Published in:Journal of biotechnology 2021-04, Vol.331, p.48-52
Main Authors: Terehova, Maria, Dzmitruk, Volha, Abashkin, Viktar, Kirakosyan, Gayane, Ghukasyan, Gevorg, Bryszewska, Maria, Pedziwiatr-Werbicka, Elzbieta, Ionov, Maksim, Gómez, Rafael, de la Mata, F. Javier, Mignani, Serge, Shi, Xiangyang, Majoral, Jean-Pierre, Sukhodola, Aleksandr, Shcharbin, Dzmitry
Format: Article
Language:English
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Summary:[Display omitted] •'Hard' and 'soft' nanoparticles differently affected phospholipase A2.•'Soft' nanoparticles formed aggregates/micelles with protein.•'Hard' nanoparticle had bimolecular interaction with protein. The interaction of nanoparticles (NP) with proteins (the so-called 'protein corona') is a huge challenge in attempting to apply them in personalized nanomedicine. We have analyzed the interaction between A) two 'soft' NPs (a cationic phosphorus dendrimer of generation 3; a cationic phosphorus amphiphilic dendron of generation 2), and B) one 'hard' nanoparticle (silver NP covered with cationic carbosilane dendritic moieties); and membrane-bound protein phospholipase A2 from bovine pancreas. The hard and soft NPs have differences in the nature of their interactions with phospholipase A2. This enzyme surrounds hard AgNP, whereas dendrimer and amphiphilic dendron form aggregates/micelles with phospholipase A2. There is a difference in action of phospholipase A2 bound to the core of dendrimer, and of micelles formed from non-covalent interactions between the amphiphilic dendron. These data are important in understanding the nature of interaction between different kinds of nanoparticles and proteins.
ISSN:0168-1656
1873-4863
DOI:10.1016/j.jbiotec.2021.03.009