Single-molecule detection with a millimetre-sized transistor

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作者
Eleonora Macchia
Kyriaki Manoli
Brigitte Holzer
Cinzia Di Franco
Matteo Ghittorelli
Fabrizio Torricelli
Domenico Alberga
Giuseppe Felice Mangiatordi
Gerardo Palazzo
Gaetano Scamarcio
Luisa Torsi
机构
[1] Università degli Studi di Bari “Aldo Moro”,Dipartimento di Chimica
[2] Istituto di Fotonica e Nanotecnologie,CNR
[3] Università degli Studi di Brescia,Dipartimento Ingegneria dell’Informazione
[4] Università degli Studi di Bari “Aldo Moro”,Dipartimento di Farmacia, Scienze del Farmaco
[5] CSGI (Centre for Colloid and Surface Science),Dipartimento di Fisica “M. Merlin”
[6] Università degli Studi di Bari – “Aldo Moro”,The Faculty of Science and Engineering
[7] Åbo Akademi University,undefined
[8] Istituto Tumori IRCCS Giovanni Paolo II,undefined
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摘要
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 1012 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.
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