| Literature DB >> 27227361 |
Carl H Naylor1, Nicholas J Kybert1, Camilla Schneier1, Jin Xi1, Gabriela Romero1, Jeffery G Saven1, Renyu Liu1, A T Charlie Johnson1.
Abstract
We demonstrate arrays of opioid biosensors based on chemical vapor deposition grown molybdenum disulfide (MoS2) field effect transistors (FETs) coupled to a computationally redesigned, water-soluble variant of the μ-opioid receptor (MOR). By transferring dense films of monolayer MoS2 crystals onto prefabricated electrode arrays, we obtain high-quality FETs with clean surfaces that allow for reproducible protein attachment. The fabrication yield of MoS2 FETs and biosensors exceeds 95%, with an average mobility of 2.0 cm(2) V(-1) s(-1) (36 cm(2) V(-1) s(-1)) at room temperature under ambient (in vacuo). An atomic length nickel-mediated linker chemistry enables target binding events that occur very close to the MoS2 surface to maximize sensitivity. The biosensor response calibration curve for a synthetic opioid peptide known to bind to the wild-type MOR indicates binding affinity that matches values determined using traditional techniques and a limit of detection ∼3 nM (1.5 ng/mL). The combination of scalable array fabrication and rapid, precise binding readout enabled by the MoS2 transistor offers the prospect of a solid-state drug testing platform for rapid readout of the interactions between novel drugs and their intended protein targets.Entities:
Keywords: biosensors; monolayer MoS2; opioids; scalable; transition-metal dichalcogenide
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Year: 2016 PMID: 27227361 PMCID: PMC4949953 DOI: 10.1021/acsnano.6b02137
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881