DNA-programmable multiplexing for scalable, renewable redox protein bio-nanoelectronics.

A universal, site-addressable DNA linking strategy is deployed for the programmable assembly of multifunctional, long-lasting redox protein nanoelectronic devices. This addressable linker, the first incorporated into a redox enzyme-nanoelectronic system, promotes versatility and renewability by allowing the reconfiguration and replacement of enzymes at will. The linker is transferable to all redox proteins due to the simple conjugation chemistry involved.

Wiring efficiency of a metallizable DNA linker for site-addressable nanobioelectronic assembly.

We report the first demonstration of DNA oligonucleotide tags used to address the site-specific assembly of multiple redox enzymes onto spatially distinct regions of a nanoelectronic platform, establishing a direct electrical contact. The resulting system constitutes a multiplexed carbon nanotube-redox protein biosensor capable of detecting varying concentrations of several different substances in real time. The efficiency and robustness of the enzyme linking scheme is explored in detail, showing a high degree of preservation of enzymatic activity and an efficient electrical contact at the enzyme-nanoelectrode interface.

Site-specific assembly of DNA and appended cargo on arrayed carbon nanotubes.

We describe a strategy that permits discrete regions of arrayed carbon nanotubes (CNTs) to be functionalized simultaneously and specifically with DNA oligonucleotides. The different chemical properties of two regions on single CNTs and orthogonal chemical coupling strategies have been exploited to derivatize CNTs within highly ordered arrays with multiple DNA sequences. Through duplex hybridization, we then targeted different DNA sequences with appended metal nanoparticles to distinct sites on the CNT architecture with precise spatial control.