Study of porphyrin-modified liquid exfoliated graphene field-effect transistors for evaluating DNA methylation degree
Literature Information
Zhongrong Wang, Shihui Hu, Fang Li, Qingjie Fan, Yunfang Jia
The applications of graphene field-effect transistors (FETs) for monitoring DNA hybridization have been widely accepted; however, for evaluating DNA methylation degree, an emerging requirement of epigenetic research, no work has been found due to the difficulties in detecting 5-methylcytosine (5mC) sites along the genomic sequence as well as counting their amount (NmC). Herein, to achieve this, a strategy for exploiting a liquid exfoliated graphene (LEG)-based FET (LEG-FET) as a sensing platform was proposed. First, LEG-FETs were prepared and activated by tetra-4-aminophenyl-porphyrin (TAPP) for anchoring single-strand DNAs (ssDNAs). Second, the 5mC sites in ssDNA were recognized by the specifically absorbed 5mC antibody (5mCab) and transduced to the changed currents (ΔIDS) by LEG-FET according to the integration of the methylation-immuno sensing principle and FET's working mechanism. Briefly, more 5mCab molecules could be captured by more 5mC sites, resulting in larger ΔIDS. The TAPP effects on LEG-FET were analyzed by SEM, Raman, AFM, and XPS characterizations as well as electronic measurements. The validity of this LEG-FET sensing platform for evaluating DNA methylation degree was proven step by step; this included the examinations of the synthesized ssDNAs with the known NmC and real ssDNA samples, whose methylation degrees were pre-determined by the gold-standard method, which is based on tedious bisulphite sequence operations and expensive mass spectrometry technology. Moreover, theoretical explanations were also provided for the sensing mechanism in the proposed DNA methylation analytical components. In conclusion, the positive and linear relations of IDS changing ratio vs. NmC as well as the detection limit of one 5mC site indicate that TAPP-modified LEG-FET can provide an alternative analytical tool to realize fast and economical DNA methylation evaluation.
Related Literature
Synthesis of octahedral Pt–Pd alloy nanoparticles for improved catalytic activity and stability in methanol electrooxidation
Young-Woo Lee, A-Ra Ko, Sang-Beom Han, Hyun-Su Kim, Kyung-Won Park
DOI: 10.1039/C0CP02167A
Singlet nuclear magnetic resonance of nearly-equivalent spins
Michael C. D. Tayler, Malcolm H. Levitt
DOI: 10.1039/C0CP02293D
Effects of conformational flexibility of alkyl chains of cations on diffusion of ions in ionic liquids
Seiji Tsuzuki, Hajime Matsumoto, Wataru Shinoda, Masuhiro Mikami
DOI: 10.1039/C0CP02087G
Towards homonuclear Jsolid-state NMR correlation experiments for half-integer quadrupolar nuclei: experimental and simulated 11B MAS spin-echo dephasing and calculated 2JBB coupling constants for lithium diborate
Nathan S. Barrow, Jonathan R. Yates, Steven A. Feller, Diane Holland, Sharon E. Ashbrook, Paul Hodgkinson, Steven P. Brown
DOI: 10.1039/C0CP02343D
Analytical theory of ideal polydisperse polymers at interfaces
Clifford E. Woodward, Jan Forsman
DOI: 10.1039/C0CP01239D
Magnetic and conduction properties in 1D organic radical materials: an ab initio inspection for a challenging quest
Martin Vérot, Jean-Baptiste Rota, Boris Le Guennic
DOI: 10.1039/C0CP02124E
Interactions of Schiff-base ligands with gold nanoparticles: structural, optical and electrocatalytic studies‡
Jose María Abad, Mónica Revenga-Parra, Tania García, Miriam Gamero, Encarnación Lorenzo, Félix Pariente
DOI: 10.1039/C0CP02164D
Picosecond X-ray absorption measurements of the ligand substitution dynamics of Fe(CO)5 in ethanol
Brian Ahr, Matthieu Chollet, Bernhard Adams, Elizabeth M. Lunny, Christopher M. Laperle, Christoph Rose-Petruck
DOI: 10.1039/C0CP01856B
Growth mechanisms of phthalocyaninenanowires induced by Au nanoparticle templates
Tobias N. Krauss, Esther Barrena
DOI: 10.1039/C0CP02191A
Structure–property relations in crystalline l-leucine obtained from calorimetry, X-rays, neutron and Raman scattering
Pedro F. Façanha Filho, Paulo T. C. Freire, José A. Lima Jr., Adenilson O. dos Santos, Paul F. Henry, Ewout Kremner, Heloisa N. Bordallo
DOI: 10.1039/C0CP02278K
You might also like
How is Ethyl 4-chlorothieno[2,3-b]pyridine-5-carboxylate (CAS: 59713-58-5) typically synthesized?
Ethyl 4-chlorothieno[2,3-b]pyridine-5-carboxylate (CAS: 59713-58-5) can be synth...
What regulatory guidelines apply to 5-Methyl-1H-indole-3-carbaldehyde (CAS: 52562-50-2)?
5-Methyl-1H-indole-3-carbaldehyde (CAS: 52562-50-2) is subject to various regula...
What are the physical and chemical properties of (1,3-Dimethyl-2,4-dioxo-1,2,3,4-tetrahydro-5-pyrimidinyl)boronic acid (CAS: 223418-73-3)?
(1,3-Dimethyl-2,4-dioxo-1,2,3,4-tetrahydro-5-pyrimidinyl)boronic acid is a white...
How should waste containing Sulfocostunolide A (CAS: 1016983-51-9) be handled?
Waste containing Sulfocostunolide A (CAS: 1016983-51-9) should be handled with c...
What precautions should be taken when handling Murraxocin (CAS: 88478-44-8)?
When handling Murraxocin (CAS: 88478-44-8), ensure proper personal protective eq...
What are the physical and chemical properties of Formvar (CAS: 63148-64-1)?
Formvar (CAS: 63148-64-1) is an alkyd resin characterized by a high molecular we...
Is (S)-4-benzyl-2-((benzyloxy)methyl)morpholine (CAS: 205242-66-6) safe?
(S)-4-benzyl-2-((benzyloxy)methyl)morpholine is generally safe when handled with...
What industries use Methyl 1-(5-bromo-2-pyrimidinyl)cyclopropanecarboxylate (CAS: 1447607-69-3)?
Methyl 1-(5-bromo-2-pyrimidinyl)cyclopropanecarboxylate (CAS: 1447607-69-3) is p...
Is 2-Methyl-1-phenyl-1-propanamine hydrochloride (CAS: 24290-47-9) safe?
2-Methyl-1-phenyl-1-propanamine hydrochloride (CAS: 24290-47-9) is generally con...
How is 3-(4-Bromophenyl)-2-methylpropanoic acid (CAS: 66735-01-1) typically synthesized?
3-(4-Bromophenyl)-2-methylpropanoic acid is synthesized through a multi-step pro...
Source Journal
Analyst

Analyst publishes analytical and bioanalytical research that reports premier fundamental discoveries and inventions, and the applications of those discoveries, unconfined by traditional discipline barriers.











![9H-Fluoren-9-ylmethyl [(2S)-1-hydroxy-3-(1H-indol-3-yl)-2-propanyl]carbamate structure 9H-Fluoren-9-ylmethyl [(2S)-1-hydroxy-3-(1H-indol-3-yl)-2-propanyl]carbamate structure](https://static.chemtradehub.com/structs/153/153815-60-2-a67d.webp)

![[2-(Benzyloxy)-3-bromo-5-methylphenyl]boronic acid structure [2-(Benzyloxy)-3-bromo-5-methylphenyl]boronic acid structure](https://static.chemtradehub.com/structs/870/870777-20-1-24ac.webp)
