Manipulating single biological objects is a major unmet challenge of biomedicine. Herein, we describe a lab-on-a-chip platform based on dielectrophoresis (DEP). The DEParray is a prototypal version consisting of 320 × 320 arrayed electrodes generating >10 000 spherical DEP cages. It allows the capture and software-guided movement to predetermined spatial coordinates of single biological objects. With the DEParray we demonstrate (a) forced interaction between a single, preselected target cell and a programmable number of either microspheres or natural killer (NK) cells, (b) on-chip immunophenotypic discrimination of individual cells based on differential rosetting with microspheres functionalized with monoclonal antibodies to an inhibitory NK cell ligand (HLA-G), (c) on-chip, real-time (few minutes) assessment of immune lysis by either visual inspection or semiautomated, time-lapse reading of a fluorescent dye released from NK cell-sensitive targets, and (d) manipulation and immunophenotyping with limiting amounts (about 500) cells. To our knowledge, this is the first report describing a DEP-based lab-on-a-chip platform for the quick, arrayed, software-guided binding of individually moved biological objects, the targeting of single cells with microspheres, and the real-time characterization of immunophenotypes. The DEParray candidates as a discovery tool for novel cell:cell interactions with no prior (immuno)phenotypic knowledge.

Programmable interactions of functionalized single bioparticles in a dielectrophoresis (DEP)-based microarray chip / Abonnenc M; Manaresi N; Borgatti M; Medoro G; Fabbri E; Romani A; Altomare L; Tartagni M; Rizzo R; Baricordi O; Tremante E; Lo Monaco E; Giacomini P; Guerrieri R; Gambari R. - In: ANALYTICAL CHEMISTRY. - ISSN 0003-2700. - STAMPA. - 85:17(2013), pp. 8219-8224. [10.1021/ac401296m]

Programmable interactions of functionalized single bioparticles in a dielectrophoresis (DEP)-based microarray chip

ROMANI, ALDO;TARTAGNI, MARCO;GUERRIERI, ROBERTO;
2013

Abstract

Manipulating single biological objects is a major unmet challenge of biomedicine. Herein, we describe a lab-on-a-chip platform based on dielectrophoresis (DEP). The DEParray is a prototypal version consisting of 320 × 320 arrayed electrodes generating >10 000 spherical DEP cages. It allows the capture and software-guided movement to predetermined spatial coordinates of single biological objects. With the DEParray we demonstrate (a) forced interaction between a single, preselected target cell and a programmable number of either microspheres or natural killer (NK) cells, (b) on-chip immunophenotypic discrimination of individual cells based on differential rosetting with microspheres functionalized with monoclonal antibodies to an inhibitory NK cell ligand (HLA-G), (c) on-chip, real-time (few minutes) assessment of immune lysis by either visual inspection or semiautomated, time-lapse reading of a fluorescent dye released from NK cell-sensitive targets, and (d) manipulation and immunophenotyping with limiting amounts (about 500) cells. To our knowledge, this is the first report describing a DEP-based lab-on-a-chip platform for the quick, arrayed, software-guided binding of individually moved biological objects, the targeting of single cells with microspheres, and the real-time characterization of immunophenotypes. The DEParray candidates as a discovery tool for novel cell:cell interactions with no prior (immuno)phenotypic knowledge.
2013
Programmable interactions of functionalized single bioparticles in a dielectrophoresis (DEP)-based microarray chip / Abonnenc M; Manaresi N; Borgatti M; Medoro G; Fabbri E; Romani A; Altomare L; Tartagni M; Rizzo R; Baricordi O; Tremante E; Lo Monaco E; Giacomini P; Guerrieri R; Gambari R. - In: ANALYTICAL CHEMISTRY. - ISSN 0003-2700. - STAMPA. - 85:17(2013), pp. 8219-8224. [10.1021/ac401296m]
Abonnenc M; Manaresi N; Borgatti M; Medoro G; Fabbri E; Romani A; Altomare L; Tartagni M; Rizzo R; Baricordi O; Tremante E; Lo Monaco E; Giacomini P; Guerrieri R; Gambari R
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/184303
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