TY - JOUR
T1 - Randomly positioned gold nanoparticles as fluorescence enhancers in apta-immunosensor for malaria test
AU - Minopoli, Antonio
AU - Della Ventura, Bartolomeo
AU - Campanile, Raffaele
AU - Tanner, Julian A.
AU - Offenhäusser, Andreas
AU - Mayer, Dirk
AU - Velotta, Raffaele
PY - 2021
Y1 - 2021
N2 - A plasmon-enhanced fluorescence-based antibody-aptamer biosensor — consisting of gold nanoparticles randomly immobilized onto a glass substrate via electrostatic self-assembly — is described for specific detection of proteins in whole blood. Analyte recognition is realized through a sandwich scheme with a capture bioreceptor layer of antibodies — covalently immobilized onto the gold nanoparticle surface in upright orientation and close-packed configuration by photochemical immobilization technique (PIT) — and a top bioreceptor layer of fluorescently labelled aptamers. Such a sandwich configuration warrants not only extremely high specificity, but also an ideal fluorophore-nanostructure distance (approximately 10–15 nm) for achieving strong fluorescence amplification. For a specific application, we tested the biosensor performance in a case study for the detection of malaria-related marker Plasmodium falciparum lactate dehydrogenase (PfLDH). The proposed biosensor can specifically detect PfLDH in spiked whole blood down to 10 pM (0.3 ng/mL) without any sample pretreatment. The combination of simple and scalable fabrication, potentially high-throughput analysis, and excellent sensing performance provides a new approach to biosensing with significant advantages compared to conventional fluorescence immunoassays. Graphical abstract: [Figure not available: see fulltext.]
AB - A plasmon-enhanced fluorescence-based antibody-aptamer biosensor — consisting of gold nanoparticles randomly immobilized onto a glass substrate via electrostatic self-assembly — is described for specific detection of proteins in whole blood. Analyte recognition is realized through a sandwich scheme with a capture bioreceptor layer of antibodies — covalently immobilized onto the gold nanoparticle surface in upright orientation and close-packed configuration by photochemical immobilization technique (PIT) — and a top bioreceptor layer of fluorescently labelled aptamers. Such a sandwich configuration warrants not only extremely high specificity, but also an ideal fluorophore-nanostructure distance (approximately 10–15 nm) for achieving strong fluorescence amplification. For a specific application, we tested the biosensor performance in a case study for the detection of malaria-related marker Plasmodium falciparum lactate dehydrogenase (PfLDH). The proposed biosensor can specifically detect PfLDH in spiked whole blood down to 10 pM (0.3 ng/mL) without any sample pretreatment. The combination of simple and scalable fabrication, potentially high-throughput analysis, and excellent sensing performance provides a new approach to biosensing with significant advantages compared to conventional fluorescence immunoassays. Graphical abstract: [Figure not available: see fulltext.]
KW - Antibody-aptamer biosensor
KW - Gold nanoparticle array
KW - Malaria marker
KW - Nanoplasmonics
KW - Photochemical immobilization technique
KW - Plasmon-enhanced fluorescence
KW - Antibody-aptamer biosensor
KW - Gold nanoparticle array
KW - Malaria marker
KW - Nanoplasmonics
KW - Photochemical immobilization technique
KW - Plasmon-enhanced fluorescence
UR - https://publicatt.unicatt.it/handle/10807/314251
UR - https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85101052224&origin=inward
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85101052224&origin=inward
U2 - 10.1007/s00604-021-04746-9
DO - 10.1007/s00604-021-04746-9
M3 - Article
SN - 0026-3672
VL - 188
SP - 1
EP - 9
JO - Mikrochimica Acta
JF - Mikrochimica Acta
IS - 3
ER -