Evidence map›Paper›PMID 30178301›Full record

ArticleMikrochimica acta2018

DNAzyme-embedded hyperbranched DNA dendrimers as signal amplifiers for colorimetric determination of nucleic acids.

Hadi Ravan, Tahereh Fozooni, Mojdeh Amandadi, Hosseinali Sasan, Akram Norouzi

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Article in Mikrochimica acta, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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5 authors.

Hadi RavanDepartment of Biology, Faculty of Sciences, Shahid Bahonar University of Kerman, Kerman, 7616914111, Iran. ravan@uk.ac.ir.ORCID 0000-0001-8560-4900
Tahereh FozooniDepartment of Biology, Faculty of Sciences, Shahid Bahonar University of Kerman, Kerman, 7616914111, Iran.
Mojdeh AmandadiDepartment of Biology, Faculty of Sciences, Shahid Bahonar University of Kerman, Kerman, 7616914111, Iran.
Hosseinali SasanDepartment of Biology, Faculty of Sciences, Shahid Bahonar University of Kerman, Kerman, 7616914111, Iran.
Akram NorouziDepartment of Clinical Biochemistry, School of Medicine, Kerman University of Medical Sciences, Kerman, 7616913555, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A DNAzyme-embedded hyperbranched DNA dendrimer is used as a colorimetric signal amplifier in an ultrasensitive detection scheme for nucleic acids. The hyperbranched DNA dendrimers were constructed by single-step autonomous self-assembly of three structure-free DNA monomers. A cascade of self-assembly reactions between the first and second strands leads to the formation of linear DNA concatemers containing overhang flank fragments. The third strand, which bears a peroxidase-mimicking DNAzyme domain, serves as a bridge to trigger self-assembly between the first and second strands across the side chain direction. This results in a chain branching growth of the DNAzyme-embedded DNA dendrimer. This signal amplifier was incorporated into the streptavidin-biotin detection system which comprises an adaptor oligonucleotide and a biotinylated capture probe. The resulting platform is capable of detecting a nucleic acid target with an LOD as low as 0.8 fM. Such sensitivity is comparable if not superior to most of the reported enzyme-free (and even enzyme-assisted) signal amplification strategies. The DNA dendrimer based method is expected to provide a universal platform for extraordinary signal enhancement in detecting other nucleic acid biomarkers by altering the respective sequences of adaptor and capture probe. Graphical abstract Schematic of an assembly of a DNAzyme-embedded hyperbranched DNA dendrimer which operates as a signal amplifier for nucleic acids detection. The nanostructure is constructed by autonomous self-assembly of three DNA monomers. Colored letters represent each domain, and complementary domains are marked by asterisk. Domain d represents the DNAzyme sequence.

Indexed as

Biosensing TechniquesColorimetryDendrimersDNADNA, CatalyticLimit of DetectionDendrimersDNADNA, CatalyticDNA concatemersDNA detectionDNA nanostructureEnzyme-free detectionLabel-free detectionPeroxidase-mimicking DNAzymeSelf-assemblySignal amplificationStreptavidin-biotin systemStructural DNA nanotechnology

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.