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Hydrazone ligation assisted DNAzyme walking nanomachine coupled with CRISPR-Cas12a for lipopolysaccharide analysis

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TLDR
In this article, hydrazone ligation assisted DNAzyme walking nanomachine is explored to couple with CRISPR-Cas12a trans-cleavage to enhance the sensitivity for target detection.
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This article is published in Analytica Chimica Acta.The article was published on 2021-08-22. It has received 10 citations till now.

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Citations
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Journal ArticleDOI

Novel non-nucleic acid targets detection strategies based on CRISPR/Cas toolboxes: A review.

TL;DR: A comprehensive review of CRISPR/Cas-based tools for non-nucleic acid target detection can be found in this article , where the authors summarize the strategies and prospects of these tools in this field.
Journal ArticleDOI

Label-Free Resonance Rayleigh Scattering Amplification for Lipopolysaccharide Detection and Logical Circuit by CRISPR/Cas12a-Driven Guanine Nanowire Assisted Non-Cross-Linking Hybridization Chain Reaction.

TL;DR: In this paper , a CRISPR-derived resonance Rayleigh scattering (RRS) amplification strategy and logical circuit based on a guanine nanowire (G-wire) assisted non-cross-linking hybridization chain reaction (GWancHCR) for label-free detection of lipopolysaccharide (LPS).
Journal ArticleDOI

CRISPR/Cas12a system responsive DNA hydrogel for label-free detection of non-glucose targets with a portable personal glucose meter.

TL;DR: In this paper , a Personal Glucose Meter (PGM) was used for sensitive detection of non-glucose targets: N-gene and PCB77, respectively.
Journal ArticleDOI

Aptamer-based CRISPR-Cas powered diagnostics of diverse biomarkers and small molecule targets

TL;DR: In this paper , the authors review current advances in aptamer-based CRISPR-Cas sensors for point-of-care setting diagnostics and provide novel insights into developing CRISpl-Cas-based sensors using ssDNA aptamers with high efficiency and specificity.
Journal ArticleDOI

Magnetism-Controllable Catalytic Activity of DNAzyme.

TL;DR: This system provides a reusable platform for the control of enzyme catalytic activity through magnetism, which provides guidance for further application in some related scientific research, especially the regulation of the activity of conformation-dependent polymers (DNAzymes, aptamers, and peptides).
References
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Journal ArticleDOI

CRISPR-Cas12a target binding unleashes indiscriminate single-stranded DNase activity

TL;DR: It is shown that RNA-guided DNA binding unleashes indiscriminate single-stranded DNA cleavage activity by Cas12a that completely degrades ssDNA molecules, which is also a property of other type V CRISPR-Cas12 enzymes.
Journal ArticleDOI

Nanoparticle Probes for the Detection of Cancer Biomarkers, Cells, and Tissues by Fluorescence

TL;DR: Overcoming Limitations in Nanoparticle Drug Delivery: Triggered, Intravascular Release to Improve Drug Penetration into Tumors and Design Considerations for Tumour-Targeted Nanoparticles.
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Exploring the Trans-Cleavage Activity of CRISPR-Cas12a (cpf1) for the Development of a Universal Electrochemical Biosensor.

TL;DR: The first CRISPR Cas12a (cpf1) based electrochemical biosensor (E-CRISPR) is reported, which is more cost-effective and portable comparing with optical transduction based biosensing systems and could be a powerful enabler for wide developments of portable, accurate, and cost-efficient point-of-care diagnostic systems.
Journal ArticleDOI

Enzyme-Powered Three-Dimensional DNA Nanomachine for DNA Walking, Payload Release, and Biosensing

TL;DR: A DNA nanomachine, built from a DNA-functionalized gold nanoparticle (DNA-AuNP), which moves a DNA walker along a three-dimensional (3-D) DNA- AuNP track and executes the task of releasing payloads, which allows it to be tailored into a DNA nanosensor that is able to achieve rapid, isothermal, and homogeneous signal amplification for specific nucleic acids in both buffer and a complicated biomatrix.
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