Label-free and reagentless electrochemical detection of PCR fragments using self-assembled quinone derivative monolayer: application to Mycobacterium tuberculosis

Autor: Peter E. Nielsen, Edgar Abadia, Minh-Chau Pham, Q.D. Zhang, Benoît Piro, Gregory March, L.V. Hai, L.D. Tran, Christophe Sola, S. Reisberg, Vincent Noël
Přispěvatelé: Institut de génétique et microbiologie [Orsay] (IGM), Université Paris-Sud - Paris 11 (UP11)-Centre National de la Recherche Scientifique (CNRS)
Jazyk: angličtina
Rok vydání: 2012
Předmět:
MESH: Mycobacterium tuberculosis
Base Pair Mismatch
Oligonucleotides
02 engineering and technology
Biosensing Techniques
MESH: Base Sequence
01 natural sciences
Polymerase Chain Reaction
law.invention
MESH: Nucleic Acid Hybridization
chemistry.chemical_compound
law
MESH: Oligonucleotides
Electrochemistry
Polymerase chain reaction
Quinones
Nucleic Acid Hybridization
General Medicine
021001 nanoscience & nanotechnology
MESH: Electrochemical Techniques
3. Good health
[SDV.MP]Life Sciences [q-bio]/Microbiology and Parasitology
0210 nano-technology
MESH: Biosensing Techniques
Biotechnology
DNA
Bacterial

Biomedical Engineering
Biophysics
Biology
010402 general chemistry
Sensitivity and Specificity
MESH: Quinones
Mycobacterium tuberculosis
Nucleic acid thermodynamics
[SDV.BBM]Life Sciences [q-bio]/Biochemistry
Molecular Biology

Sulfhydryl Compounds
MESH: Sulfhydryl Compounds
MESH: Base Pair Mismatch
Base Sequence
Oligonucleotide
MESH: Polymerase Chain Reaction
Electrochemical Techniques
biology.organism_classification
Molecular biology
Combinatorial chemistry
MESH: DNA
Bacterial

MESH: Sensitivity and Specificity
0104 chemical sciences
chemistry
Hydroxynaphthoquinone
Biosensor
DNA
Zdroj: Biosensors and Bioelectronics
Biosensors and Bioelectronics, Elsevier, 2012, 32 (1), pp.163-8. ⟨10.1016/j.bios.2011.11.048⟩
ISSN: 0956-5663
DOI: 10.1016/j.bios.2011.11.048⟩
Popis: International audience; We report a signal-on, label-free and reagentless electrochemical DNA biosensor, based on a mixed self-assembled monolayer of thiolated hydroxynaphthoquinone and thiolated oligonucleotide. Electrochemical changes resulting from hybridization were evidenced with oligonucleotide targets (as models), as well as with polymerase chain reaction (PCR) products related to different lineages of Mycobacterium tuberculosis strains. With pure oligonucleotides, this system achieves high sensitivity (∼300 pM of DNA target, i.e. 30 fmol in a 100 μL sample) and excellent selectivity, allowing to detect a single mismatch on a sequence of 20 bases. With PCR products, current changes are specific to the bacterial strain from which the PCR fragment is produced. In addition, the sensor response is of the signal-on type, giving a positive signal change upon hybridization, and therefore does not suffer from false positive responses due to non-specific adsorption of DNA.
Databáze: OpenAIRE