
Cell Reports Methods, Journal Year: 2024, Volume and Issue: unknown, P. 100912 - 100912
Published: Dec. 1, 2024
Language: Английский
Cell Reports Methods, Journal Year: 2024, Volume and Issue: unknown, P. 100912 - 100912
Published: Dec. 1, 2024
Language: Английский
Biosensors and Bioelectronics, Journal Year: 2024, Volume and Issue: 264, P. 116671 - 116671
Published: Aug. 17, 2024
Language: Английский
Citations
8Coordination Chemistry Reviews, Journal Year: 2024, Volume and Issue: 513, P. 215895 - 215895
Published: May 4, 2024
Language: Английский
Citations
7ACS Synthetic Biology, Journal Year: 2024, Volume and Issue: 13(7), P. 2166 - 2176
Published: June 12, 2024
CRISPR-based diagnostics use the CRISPR-Cas system
Language: Английский
Citations
6Sensors and Actuators B Chemical, Journal Year: 2024, Volume and Issue: 417, P. 136196 - 136196
Published: June 25, 2024
Language: Английский
Citations
6Coordination Chemistry Reviews, Journal Year: 2024, Volume and Issue: 518, P. 216083 - 216083
Published: July 23, 2024
Language: Английский
Citations
6ACS Sensors, Journal Year: 2024, Volume and Issue: 9(11), P. 5665 - 5682
Published: Nov. 11, 2024
Rapid and accurate detection is a prerequisite for precise clinical diagnostics, ensuring food safety, facilitating biotechnological applications. The Argonaute system, as cutting-edge technique, has been successfully repurposed in biosensing beyond the CRISPR/Cas system (clustered regularly interspaced short palindromic repeats CRISPR-associated proteins), which extensively researched, but recognition of PAM sequences remains restricted. Argonaute, programmable target-activated nuclease, fabricating novel methods due to its unparalleled biological features. In this comprehensive review, we initially elaborate on current nucleic acid testing nucleases, followed by delving into structure nuclease activity system. advantages compared with are highlighted discussed. Furthermore, summarize applications Argonaute-based provide an in-depth analysis future perspectives challenges. Recent research demonstrated that innovative rapidly advancing technology can overcome limitations existing potentially replace them. summary, implementation integration other technologies hold promise developing customized intelligent across various aspects.
Language: Английский
Citations
6Journal of Agricultural and Food Chemistry, Journal Year: 2024, Volume and Issue: 72(19), P. 11195 - 11204
Published: April 2, 2024
Genetically modified crops (GMCs) have been discussed due to unknown safety, and thus, it is imperative develop an effective detection technology. CRISPR/Cas deemed a burgeoning technology for nucleic acid detection. Herein, we developed novel method the first time, which combined thermostable Cas12b with loop-mediated isothermal amplification (LAMP), detect genetically (GM) soybeans in customized one-pot vessel. In our method, LAMP-specific primers were used amplify cauliflower mosaic virus 35S promoter (CaMV35S) of GM soybean samples. The corresponding amplicons activated
Language: Английский
Citations
5Trends in biotechnology, Journal Year: 2024, Volume and Issue: 42(11), P. 1410 - 1426
Published: July 20, 2024
Language: Английский
Citations
5Diagnostic Microbiology and Infectious Disease, Journal Year: 2024, Volume and Issue: 109(2), P. 116252 - 116252
Published: March 8, 2024
Language: Английский
Citations
4Critical Reviews in Biotechnology, Journal Year: 2024, Volume and Issue: unknown, P. 1 - 28
Published: Sept. 22, 2024
CRISPR-based diagnostics (CRISPR/Dx) have revolutionized the field of molecular diagnostics. It enables home self-test, field-deployable, and point-of-care testing (POCT). Despite great potential CRISPR/Dx in diagnoses biologically complex diseases, preamplification template often is required for sensitive detection low-abundance nucleic acids. Various amplification-free systems were recently developed to enhance signal at sufficient sensitivity. Broadly, these are classified into five groups depending on enhancement strategies employed: CRISPR/Cas12a and/or CRISPR/Cas13a integrated with: (1) other catalytic enzymes (Cas14a, Csm6, Argonaute, duplex-specific nuclease, nanozyme, or T7 exonuclease), (2) rational-designed oligonucleotides (multivalent aptamer, tetrahedral DNA framework, RNA G-quadruplexes, roller machine, switchable-caged guide RNA, hybrid locked RNA/DNA probe, hybridized cascade "U" rich stem-loop RNA), (3) nanomaterials (nanophotonic structure, gold nanoparticle, micromotor, microbeads), (4) electrochemical piezoelectric plate biosensors (SERS nanoprobes, graphene field-effect transistor, redox primer exchange reaction), (5) cutting-edge technology platforms (digital bioanalysis, droplet microfluidic, smartphone camera, single nanoparticle counting). Herein, we critically discuss advances, pitfalls future perspectives acids detection. The continued refinement will pave road rapid, cost-effective, ultrasensitive, ultraspecific on-site without resorting target amplification, with ultimate goal establishing as paragon
Language: Английский
Citations
4