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Single-molecule detection with a millimetre-sized transistor

Label-free single-molecule detection has been achieved so far by funnelling a large number of ligands into a sequence of single-binding events with few recognition elements host on nanometric transducers. Such approaches are inherently unable to sense a cue in a bulk milieu. Conceptualizing cells’ a...

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Detalles Bibliográficos
Autores principales: Macchia, Eleonora, Manoli, Kyriaki, Holzer, Brigitte, Di Franco, Cinzia, Ghittorelli, Matteo, Torricelli, Fabrizio, Alberga, Domenico, Mangiatordi, Giuseppe Felice, Palazzo, Gerardo, Scamarcio, Gaetano, Torsi, Luisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6089965/
https://www.ncbi.nlm.nih.gov/pubmed/30104563
http://dx.doi.org/10.1038/s41467-018-05235-z
Descripción
Sumario:Label-free single-molecule detection has been achieved so far by funnelling a large number of ligands into a sequence of single-binding events with few recognition elements host on nanometric transducers. Such approaches are inherently unable to sense a cue in a bulk milieu. Conceptualizing cells’ ability to sense at the physical limit by means of highly-packed recognition elements, a millimetric sized field-effect-transistor is used to detect a single molecule. To this end, the gate is bio-functionalized with a self-assembled-monolayer of 10(12) capturing anti-Immunoglobulin-G and is endowed with a hydrogen-bonding network enabling cooperative interactions. The selective and label-free single molecule IgG detection is strikingly demonstrated in diluted saliva while 15 IgGs are assayed in whole serum. The suggested sensing mechanism, triggered by the affinity binding event, involves a work-function change that is assumed to propagate in the gating-field through the electrostatic hydrogen-bonding network. The proposed immunoassay platform is general and can revolutionize the current approach to protein detection.