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Published February 21, 2013 | Supplemental Material
Journal Article Open

Micromotor-based lab-on-chip immunoassays

Abstract

Here we describe the first example of using self-propelled antibody-functionalized synthetic catalytic microengines for capturing and transporting target proteins between the different reservoirs of a lab-on-a-chip (LOC) device. A new catalytic polymer/Ni/Pt microtube engine, containing carboxy moieties on its mixed poly(3,4-ethylenedioxythiophene) (PEDOT)/COOH–PEDOT polymeric outermost layer, is further functionalized with the antibody receptor to selectively recognize and capture the target protein. The new motor-based microchip immunoassay operations are carried out without any bulk fluid flow, replacing the common washing steps in antibody-based protein bioassays with the active transport of the captured protein throughout the different reservoirs, where each step of the immunoassay takes place. A first microchip format involving an 'on-the-fly' double-antibody sandwich assay (DASA) is used for demonstrating the selective capture of the target protein, in the presence of excess of non-target proteins. A secondary antibody tagged with a polymeric-sphere tracer allows the direct visualization of the binding events. In a second approach the immuno-nanomotor captures and transports the microsphere-tagged antigen through a microchannel network. An anti-protein-A modified microengine is finally used to demonstrate the selective capture, transport and convenient label-free optical detection of a Staphylococcus aureus target bacteria (containing proteinA in its cell wall) in the presence of a large excess of non-target (Saccharomyces cerevisiae) cells. The resulting nanomotor-based microchip immunoassay offers considerable potential for diverse applications in clinical diagnostics, environmental and security monitoring fields.

Additional Information

© 2013 Royal Society of Chemistry. Received 21st August 2012 , Accepted 11th October 2012. First published on 23rd October 2012. This work was supported by the U.S. DTRA Grant HDTRA1-13-1-0002 and NATO Science for Peace and Security Program (SfP 983807). M. G. G., J.O. and M. G. acknowledge financial support from the University of Alcalá (Madrid), the Government of Catalonia and the Spanish MICINN, respectively. W.G. is a Howard Hughes Medical Institute International Student Research fellow. We also thank Allan Cortés and Ashley Pourazary for their support in the experiments.

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Created:
August 19, 2023
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