2018
Prussian blue nanoparticles as nanozyme label in immunoassays
ČUNDERLOVÁ, Veronika, Antonín HLAVÁČEK, Zdeněk FARKA, Veronika HORÁČKOVÁ, Zuzana MIKUŠOVÁ et. al.Základní údaje
Originální název
Prussian blue nanoparticles as nanozyme label in immunoassays
Autoři
ČUNDERLOVÁ, Veronika (203 Česká republika, domácí), Antonín HLAVÁČEK (203 Česká republika, domácí), Zdeněk FARKA (203 Česká republika, domácí), Veronika HORÁČKOVÁ (203 Česká republika, domácí), Zuzana MIKUŠOVÁ (703 Slovensko, domácí) a Petr SKLÁDAL (203 Česká republika, garant, domácí)
Vydání
CEITEC PhD and Postdoc Retreat, 2018
Další údaje
Jazyk
angličtina
Typ výsledku
Konferenční abstrakt
Obor
10406 Analytical chemistry
Stát vydavatele
Česká republika
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Kód RIV
RIV/00216224:14740/18:00102730
Organizační jednotka
Středoevropský technologický institut
ISBN
978-80-210-8941-9
Klíčová slova anglicky
Prussian blue nanoparticle; Enzyme biomimic; Bioconjugation; Sandwich immunoassay; Salmonella; Human serum albumin
Štítky
Změněno: 26. 3. 2019 15:18, Mgr. Pavla Foltynová, Ph.D.
Anotace
V originále
Enzymes represent the most often used labels for amplification of signal in immunoassays due to their high catalytic efficiency. However, natural enzymes suffer from several disadvantages, e.g. they are easily denatured and their production and purification is generally complicated and time-consuming. Contrary, inorganic catalytic nanoparti-cles (nanozymes) offer easy and fast synthesis from commonly used chemicals. One of them are Prussian blue nanoparticles (PBNPs), which are nanozymes composed of coordination polymer of Fe4[Fe(CN)6]3. PBNPs contain the Fe3+/Fe2+ redox couple on the surface, which is also responsible for catalytic activity of peroxidases. PBNPs show high efficiency in catalyzing the oxidation of colorless 3,3,5,5-tetramethylbenzi-dine in the presence of H2O2 to form intensively blue product. We have prepared PBNPs with turnover number of 20 000 s-1 towards TMB oxidation, which is the highest value reported for nanoparticles of a size comparable to common proteins. We have also introduced the method for conjugation of PBNPs with antibody and utilization of the conjugate as a catalytic label in sandwich nanozyme-linked immunosorbent assay (NLISA). The practical applicability of NLISA was demonstrated by detection of different antigens, human serum albumin in urine and Salmonella Typhimurium in milk with limit of detection of 1.2 ng mL1 and 6·10^3 CFU mL1 respectively.
Návaznosti
LQ1601, projekt VaV |
|