bridging-the-bio-electronic-interface-with-biofabrication

Bridging the Bio-Electronic Interface with Biofabrication

Advancements in lab-on-a-chip technology promise to revolutionize both research and medicine through lower costs, better sensitivity, portability, and ...

a-microfluidic-based-electrochemical-biochip-for-label-free-dna

A Microfluidic-based Electrochemical Biochip for Label-free DNA Hybridization Analysis

Miniaturization of analytical benchtop procedures into the micro-scale provides significant advantages in regards to reaction time, cost, and integration ...

University of Maryland 

Redox cycling provides a mechanism to amplify electrochemical signals for analyte detection. Previous studies have shown that diverse mediators/shuttles can engage in redox-cycling reactions with a biobased redox capacitor that is fabricated by grafting redox-active catechols onto a chitosan film. Here, we report that redox cycling with this catechol-chitosan redox capacitor can amplify electrochemical signals for detecting a redox-active bacterial metabolite. Specifically, we studied the redox-active bacterial metabolite pyocyanin that is reported to be a virulence factor and signaling molecule for the opportunistic pathogen P. aeruginosa. We demonstrate that redox cycling can amplify outputs from various electrochemical methods (cyclic voltammetry, chronocoulometry, and differential pulse voltammetry) and can lower the detection limit of pyocyanin to 50 nM. Further, the compatibility of this biobased redox capacitor allows the in situ monitoring of the production of redox-active metabolites (e.g., pyocyanin) during the course of P. aeruginosa cultivation. We anticipate that the amplified output of redox-active virulence factors should permit an earlier detection of life-threatening infections by the opportunistic pathogen P. aeruginosa while the "bio-compatibility" of this measurement approach should facilitate in situ study of the spatiotemporal dynamics of bacterial redox signaling.

Amplified and in situ detection of redox-active metabolite using a biobased redox capacitor.

Phenolics are among the most abundant redox-active organics in nature, but the intractability of phenolic materials (e.g., melanin) has precluded study of their biological activities and functions. Previous studies demonstrated that a model abiotic catecholic matrix can rapidly exchange electrons with biological oxidants and reductants without the need for enzymes. Here, a novel electrochemically based reverse engineering approach was employed to probe redox interactions between this model matrix and a population of bacteria. Specifically, this method employs redox-active natural products (e.g., pyocyanin) to shuttle electrons between the bacteria and the abiotic matrix, and imposed oscillating potential inputs to engage redox-cycling mechanisms that switch the matrix's redox state. The oscillating output currents were observed to be amplified, gated, and partially rectified, while the overall magnitude and direction of electron flow across the matrix depended on the biological and environmental context. These response characteristics support hypotheses that natural phenolic materials may be integral to extracellular electron transport for processes that include anaerobic respiration, redox signaling, and redox-effector action.

Reverse engineering to suggest biologically relevant redox activities of phenolic materials.

Microelectronic devices that contain biological components are typically used to interrogate biology rather than control biological function. Patterned assemblies of proteins and cells have, however, been used for in vitro metabolic engineering, where coordinated biochemical pathways allow cell metabolism to be characterized and potentially controlled on a chip. Such devices form part of technologies that attempt to recreate animal and human physiological functions on a chip and could be used to revolutionize drug development. These ambitious goals will, however, require new biofabrication methodologies that help connect microelectronics and biological systems and yield new approaches to device assembly and communication. Here, we report the electrically mediated assembly, interrogation and control of a multi-domain fusion protein that produces a bacterial signalling molecule. The biological system can be electrically tuned using a natural redox molecule, and its biochemical response is shown to provide the signalling cues to drive bacterial population behaviour. We show that the biochemical output of the system correlates with the electrical input charge, which suggests that electrical inputs could be used to control complex on-chip biological processes.

Tanya Gordonov

Fischell Department of Bioengineering

University of Maryland

Bridging the Bio-Electronic Interface with Biofabrication

A Microfluidic-based Electrochemical Biochip for Label-free DNA Hybridization Analysis

Tanya Gordonov

.css-o250i3{font-size:18px;font-family:Open Sans,sans-serif;line-height:21.6px;}Fischell Department of Bioengineering

University of Maryland

Bridging the Bio-Electronic Interface with Biofabrication

A Microfluidic-based Electrochemical Biochip for Label-free DNA Hybridization Analysis

Fischell Department of Bioengineering