» Articles » PMID: 27797479

The Intracellular Destiny of the Protein Corona: A Study on Its Cellular Internalization and Evolution

Overview
Journal ACS Nano
Specialty Biotechnology
Date 2016 Nov 3
PMID 27797479
Citations 57
Authors
Affiliations
Soon will be listed here.
Abstract

It has been well established that the early stages of nanoparticle-cell interactions are governed, at least in part, by the layer of proteins and other biomolecules adsorbed and slowly exchanged with the surrounding biological media (biomolecular corona). Subsequent to membrane interactions, nanoparticles are typically internalized into the cell and trafficked along defined pathways such as, in many cases, the endolysosomal pathway. Indeed, if the original corona is partially retained on the nanoparticle surface, the biomolecules in this layer may play an important role in determining subsequent cellular processing. In this work, using a combination of organelle separation and fluorescence labeling of the initial extracellular corona, we clarify its intracellular evolution as nanoparticles travel within the cell. We show that specific proteins present in the original protein corona are retained on the nanoparticles until they accumulate in lysosomes, and, once there, they are degraded. We also report on how different bare surfaces (amino and carboxyl modified) affect the details of this evolution. One overarching discovery is that the same serum proteins can exhibit different intracellular processing when carried inside cells by nanoparticles, as components of their corona, compared to what is observed when they are transported freely from the extracellular medium.

Citing Articles

Structuring lipid nanoparticles, DNA, and protein corona into stealth bionanoarchitectures for in vivo gene delivery.

Renzi S, Digiacomo L, Pozzi D, Quagliarini E, Vulpis E, Giuli M Nat Commun. 2024; 15(1):9119.

PMID: 39438484 PMC: 11496629. DOI: 10.1038/s41467-024-53569-8.


Innovative optical imaging strategies for monitoring immunotherapy in the tumor microenvironments.

Um-E-Kalsoom , Wang S, Qu J, Liu L Cancer Med. 2024; 13(19):e70155.

PMID: 39387259 PMC: 11465031. DOI: 10.1002/cam4.70155.


Peptide-coated DNA nanostructures as a platform for control of lysosomal function in cells.

Elblova P, Lunova M, Henry S, Tu X, Cale A, Dejneka A Chem Eng J. 2024; 498.

PMID: 39372137 PMC: 11448966. DOI: 10.1016/j.cej.2024.155633.


Protein corona dynamicity contributes to biological destiny disparities of nanoparticles.

Zhang L, Sun T, Gong M, Zhou C, Zhao Y, Zhang W Mater Today Bio. 2024; 28:101215.

PMID: 39221215 PMC: 11364921. DOI: 10.1016/j.mtbio.2024.101215.


Stepwise-targeting and hypoxia-responsive liposome AMVY@NPs carrying siYAP and verteporfin for glioblastoma therapy.

Qi J, Zhang L, Ren Z, Yuan Y, Yu J, Zhang Y J Nanobiotechnology. 2024; 22(1):495.

PMID: 39164753 PMC: 11334488. DOI: 10.1186/s12951-024-02776-y.