Interactions of DNA with graphene and sensing applications of graphene field-effect transistor devices: A review |
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Authors: | Nathaniel S. GreenAuthor Vitae Michael L. Norton |
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Affiliation: | Department of Chemistry, Marshall University, One John Marshall Drive, Huntington, WV 25755, United States |
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Abstract: | Graphene field-effect transistors (GFET) have emerged as powerful detection platforms enabled by the advent of chemical vapor deposition (CVD) production of the unique atomically thin 2D material on a large scale. DNA aptamers, short target-specific oligonucleotides, are excellent sensor moieties for GFETs due to their strong affinity to graphene, relatively short chain-length, selectivity, and a high degree of analyte variability. However, the interaction between DNA and graphene is not fully understood, leading to questions about the structure of surface-bound DNA, including the morphology of DNA nanostructures and the nature of the electronic response seen from analyte binding. This review critically evaluates recent insights into the nature of the DNA graphene interaction and its affect on sensor viability for DNA, small molecules, and proteins with respect to previously established sensing methods. We first discuss the sorption of DNA to graphene to introduce the interactions and forces acting in DNA based GFET devices and how these forces can potentially affect the performance of increasingly popular DNA aptamers and even future DNA nanostructures as sensor substrates. Next, we discuss the novel use of GFETs to detect DNA and the underlying electronic phenomena that are typically used as benchmarks for characterizing the analyte response of these devices. Finally, we address the use of DNA aptamers to increase the selectivity of GFET sensors for small molecules and proteins and compare them with other, state of the art, detection methods. |
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Keywords: | GFET, graphene field-effect transistor CVD, chemical vapor deposition 2D, two-dimensional DNA, deoxyribonucleic acid SMFS, single molecule force microscopy ssDNA, single-stranded deoxyribonucleic acid AFM, atomic force microscopy dsDNA, double-stranded deoxyribonucleic acid PDGF, platelet derived growth factor SAMs, self-assembled monolayers HOPG, highly ordered pyrolytic graphite SA, streptavidin GO, graphene oxide RIE, reactive ion etching rGO, reduced graphene oxide XPS, X-ray photoelectron spectroscopy NrGO, nitrogen doped graphene oxide VCNP, conductance neutral point LOD, limit of detection GCE, glassy carbon electrode ppm, parts per million ppb, parts per billion MIPK, methyl isopropyl ketone CMUT, capacitive micromachined ultrasonic transducer DMMP, dimethyl methylphosphonate ATP, adenosine triphosphate TMN, tris magnesium sodium buffer PBS, phosphate buffered saline DPV, differential pulse voltammetry SERS, surface enhanced Raman spectroscopy FET, field-effect transistor PA, protective antigen pI, isoelectric point PBASE, pyrenebutanoic acid succinimidyl ester TBA, thrombin binding aptamer DAN, 1,5-diaminonapthalene VGEF, vascular endothelial growth factor MES, 2-(N-morpholino)ethanesulfonic acid IgE, immunoglobulin E |
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