2022
DOI: 10.1016/j.aca.2022.340439
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CRISPR/Cas12a system responsive DNA hydrogel for label-free detection of non-glucose targets with a portable personal glucose meter

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Cited by 16 publications
(10 citation statements)
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“…This method allows for a rapid, sensitive and specific analysis of DNA and provides a new pathway for oligonucleic acids amplification. Recently, a large amount of research has focused on using the CRISPR-Cas12a system in amplifying biomolecular assays. For example, Lu et al used an aptamer and DNAzyme regulated CRISPR-Cas12a sensor for fluorometric diagnosis of the non-nucleic acid target . Dai et al constructed a universal electrochemical biosensor based on CRISPR-Cas12a system .…”
mentioning
confidence: 99%
“…This method allows for a rapid, sensitive and specific analysis of DNA and provides a new pathway for oligonucleic acids amplification. Recently, a large amount of research has focused on using the CRISPR-Cas12a system in amplifying biomolecular assays. For example, Lu et al used an aptamer and DNAzyme regulated CRISPR-Cas12a sensor for fluorometric diagnosis of the non-nucleic acid target . Dai et al constructed a universal electrochemical biosensor based on CRISPR-Cas12a system .…”
mentioning
confidence: 99%
“…In 2022, Ma et al amplifies the detection of SARS-CoV-2 N-gene (nucleocapsid phosphoprotein gene) and PCB77 (3,3′,4,4′-tetrachlorobiphenyl) by CRISPR-responsive DNA hydrogels combined with PGM, solving the above problems. [104] Specifically, when the target gene is present, it hybridizes to the matching sequence and then undergoes cyclization and RCA process to produce a DNA product with a long repeat that binds Cas12a/sgRNA. The Cas12a is activated to cut the ssDNA cross-linkers, gel transforming sol.…”
Section: Biosensingmentioning
confidence: 99%
“…For example, Cas12a nuclease, when activated by crRNA, is capable of non-specifically cleaving long-stranded DNA at specific binding sites. Ma et al [ 66 ] designed a Cas12a/crRNA enzyme-responsive DNA hydrogel for the detection of specific genes. In the presence of target gene, Cas12a enzyme activity was activated and led to the disruption of the cross-links, thereby releasing the invertase, which converted sucrose to glucose for signal readout with a glucose meter ( Figure 3 F).…”
Section: Preparation and Classification Of Stimulus-responsive Dna Hy...mentioning
confidence: 99%
“…( F ) Schematic representation of the DNA hydrogel sensing platform for sensing N-gene via a PGM. Copyright (2022) Elsevier [ 66 ].…”
Section: Figurementioning
confidence: 99%