J 2022

Investigation of Protein Corona Formed around Biologically Produced Gold Nanoparticles

POURALI, Parastoo, Eva NEUHOFEROVA, Volha DZMITRUK a Veronika BENSON

Základní údaje

Originální název

Investigation of Protein Corona Formed around Biologically Produced Gold Nanoparticles

Autoři

POURALI, Parastoo, Eva NEUHOFEROVA, Volha DZMITRUK a Veronika BENSON

Vydání

MATERIALS, MDPI, 2022, 1996-1944

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

10400 1.4 Chemical sciences

Stát vydavatele

Švýcarsko

Utajení

není předmětem státního či obchodního tajemství

Odkazy

Impakt faktor

Impact factor: 3.400

Kód RIV

RIV/00216224:14740/22:00128760

Organizační jednotka

Středoevropský technologický institut

UT WoS

000822164200001

Klíčová slova anglicky

biologically produced gold nanoparticles; hard protein corona; capping agent; Fusarium oxysporum

Štítky

Příznaky

Mezinárodní význam, Recenzováno
Změněno: 3. 4. 2023 17:33, Mgr. Pavla Foltynová, Ph.D.

Anotace

V originále

Although there are several research articles on the detection and characterization of protein corona on the surface of various nanoparticles, there are no detailed studies on the formation, detection, and characterization of protein corona on the surface of biologically produced gold nanoparticles (AuNPs). AuNPs were prepared from Fusarium oxysporum at two different temperatures and characterized by spectrophotometry, Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), and energy-dispersive X-ray spectroscopy (EDS). The zeta potential of AuNPs was determined using a Zetasizer. AuNPs were incubated with 3 different concentrations of mouse plasma, and the hard protein corona was detected first by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and then by electrospray liquid chromatography-mass spectrometry (LC-MS). The profiles were compared to AuNPs alone that served as control. The results showed that round and oval AuNPs with sizes below 50 nm were produced at both temperatures. The AuNPs were stable after the formation of the protein corona and had sizes larger than 86 nm, and their zeta potential remained negative. We found that capping agents in the control samples contained small peptides/amino acids but almost no protein(s). After hard protein corona formation, we identified plasma proteins present on the surface of AuNPs. The identified plasma proteins may contribute to the AuNPs being shielded from phagocytizing immune cells, which makes the AuNPs a promising candidate for in vivo drug delivery. The protein corona on the surface of biologically produced AuNPs differed depending on the capping agents of the individual AuNP samples and the plasma concentration.

Návaznosti

90127, velká výzkumná infrastruktura
Název: CIISB II