CRISPR/Cas-Powered Amplification-Free Detection of Nucleic Acids: Current State of the Art, Challenges, and Futuristic Perspectives DOI
Yaru Li, Yajie Liu, Xiaoqin Tang

et al.

ACS Sensors, Journal Year: 2023, Volume and Issue: 8(12), P. 4420 - 4441

Published: Nov. 18, 2023

CRISPR/Cas system is becoming an increasingly influential technology that has been repositioned in nucleic acid detection. A preamplification step usually required to improve the sensitivity of CRISPR/Cas-based The striking biological features CRISPR/Cas, including programmability, high and sequence specificity, single-base resolution. More strikingly, target-activated trans-cleavage could act as a biocatalytic signal transductor amplifier, thereby empowering it potentially perform detection without step. reports such work are on rise, which not only scientifically significant but also promising for futuristic end-user applications. This review started with introduction methods acids diagnostics (CRISPR-Dx). Next, we objectively discussed pros cons steps CRISPR-Dx. We then illustrated highlighted recently developed strategies CRISPR/Cas-powered amplification-free can be realized through uses ultralocalized reactors, cascade reactions, ultrasensitive systems, or others. Lastly, challenges perspectives were proposed. It expected this makes researchers better understand current emerging field, provides insight designing novel CRISPR-Dx win practicable use near future.

Language: Английский

SERS-based CRISPR/Cas assay on microfluidic paper analytical devices for supersensitive detection of pathogenic bacteria in foods DOI

Jianwen Zhuang,

Zhiying Zhao,

Kai Lian

et al.

Biosensors and Bioelectronics, Journal Year: 2022, Volume and Issue: 207, P. 114167 - 114167

Published: March 17, 2022

Language: Английский

Citations

198

Advances in nucleic acid amplification techniques (NAATs): COVID-19 point-of-care diagnostics as an example DOI
Tongjia Ella Kang, Jingming Lu, Yu Tian

et al.

Biosensors and Bioelectronics, Journal Year: 2022, Volume and Issue: 206, P. 114109 - 114109

Published: Feb. 26, 2022

Language: Английский

Citations

142

Novel non-nucleic acid targets detection strategies based on CRISPR/Cas toolboxes: A review DOI
X. Cheng, Yaru Li,

Jun Kou

et al.

Biosensors and Bioelectronics, Journal Year: 2022, Volume and Issue: 215, P. 114559 - 114559

Published: July 13, 2022

Language: Английский

Citations

124

A smartphone-based visual biosensor for CRISPR-Cas powered SARS-CoV-2 diagnostics DOI Open Access
Long Ma, Lijuan Yin, Xiaoyan Li

et al.

Biosensors and Bioelectronics, Journal Year: 2021, Volume and Issue: 195, P. 113646 - 113646

Published: Sept. 23, 2021

Language: Английский

Citations

121

CRISPR‐Cas‐based detection for food safety problems: Current status, challenges, and opportunities DOI
Yaru Li, Shuli Man,

Shengying Ye

et al.

Comprehensive Reviews in Food Science and Food Safety, Journal Year: 2022, Volume and Issue: 21(4), P. 3770 - 3798

Published: July 1, 2022

Abstract Food safety is one of the biggest public issues occurring around world. Microbiological, chemical, and physical hazards can lead to food issues, which may occur at all stages supply chain. In order tackle safeguard consumer health, rapid, accurate, specific, field‐deployable detection methods meeting diverse requirements are imperative measures for assurance. CRISPR‐Cas system, a newly emerging technology, has been successfully repurposed in biosensing demonstrated huge potential establish conceptually novel with high sensitivity specificity. This review focuses on CRISPR‐Cas–based its current status specifically inspection. We firstly illustrate pending problems summarize popular methods. then describe applications Finally, challenges futuristic opportunities proposed discussed. Generally speaking, still unsatisfactory some ways such as being time‐consuming, displaying unmet specificity standards, there comparative paucity multiplexed testing POCT. Recent studies have shown that an innovative fast‐expanding could make up shortcomings existing or even replace them. To sum up, implementation integration other techniques promising desirable, expected provide “customized” “smart” inspection coming future.

Language: Английский

Citations

99

Integrating CRISPR/Cas within isothermal amplification for point-of-Care Assay of nucleic acid DOI
Limei Zhang, Hui Jiang, Zixin Zhu

et al.

Talanta, Journal Year: 2022, Volume and Issue: 243, P. 123388 - 123388

Published: March 12, 2022

Language: Английский

Citations

72

A SERS-signalled, CRISPR/Cas-powered bioassay for amplification-free and anti-interference detection of SARS-CoV-2 in foods and environmental samples using a single tube-in-tube vessel DOI Open Access
Long Ma, Wenlu Zhang, Lijuan Yin

et al.

Journal of Hazardous Materials, Journal Year: 2023, Volume and Issue: 452, P. 131195 - 131195

Published: March 11, 2023

Language: Английский

Citations

57

Advancements in CRISPR-Based Biosensing for Next-Gen Point of Care Diagnostic Application DOI Creative Commons

Akash Kumaran,

Nathan Jude Serpes,

Tisha Gupta

et al.

Biosensors, Journal Year: 2023, Volume and Issue: 13(2), P. 202 - 202

Published: Jan. 29, 2023

With the move of molecular tests from diagnostic labs to on-site testing becoming more common, there is a sudden rise in demand for nucleic acid-based tools that are selective, sensitive, flexible terrain changes, and cost-effective assist point-of-care systems large-scale screening be used remote locations cases outbreaks pandemics. CRISPR-based biosensors comprise promising new approach acid detection, which uses Cas effector proteins (Cas9, Cas12, Cas13) as extremely specialized identification components may conjunction with variety readout approaches (such fluorescence, colorimetry, potentiometry, lateral flow assay, etc.) onsite analysis. In this review, we cover some technical aspects integrating CRISPR system traditional biosensing methods amplification technologies such polymerase chain reaction (PCR), loop-mediated isothermal (LAMP), recombinase (RPA) continue elaborate on prospects developed biosensor detection major viral bacterial diseases. Within scope article, also discuss recent COVID pandemic numerous have undergone development since its advent. Finally, challenges future testing.

Language: Английский

Citations

44

CRISPR-Microfluidics Nexus: Advancing Biomedical Applications for Understanding and Detection DOI Creative Commons

ZahraSadat Razavi,

M. Soltani, Hamidreza Pazoki‐Toroudi

et al.

Sensors and Actuators A Physical, Journal Year: 2024, Volume and Issue: 376, P. 115625 - 115625

Published: June 24, 2024

The integration of CRISPR technology with microfluidic-based biosensors has greatly expanded its applications in medicine and molecular biology. This combination offers enhanced sensitivity selectivity medical diagnostics. CRISPR-powered microfluidics enables the accurate quantification DNA RNA associated diseases such as cancer, viral infections, bacterial diseases. precise targeting capabilities allow for detection specific genetic sequences, aiding early diagnosis, disease monitoring, treatment assessment. improves specificity by leveraging programmable nature coupling it signal readouts. However, challenges assay optimization, standardization, device fabrication need to be addressed. Additionally, complexity presents potential limitations terms off-target effects unintended modifications. Overall, holds tremendous diagnostics, but further research development are required fully exploit benefits clinical settings.

Language: Английский

Citations

20

On-Site Fluorescent Detection of Sepsis-Inducing Bacteria using a Graphene-Oxide CRISPR-Cas12a (GO-CRISPR) System DOI Creative Commons
Tom Kasputis, Yawen He, Qiaoqiao Ci

et al.

Analytical Chemistry, Journal Year: 2024, Volume and Issue: 96(6), P. 2676 - 2683

Published: Jan. 30, 2024

Sepsis is an extremely dangerous medical condition that emanates from the body's response to a pre-existing infection. Early detection of sepsis-inducing bacterial infections can greatly enhance treatment process and potentially prevent onset sepsis. However, current point-of-care (POC) sensors are often complex costly or lack ideal sensitivity for effective detection. Therefore, it crucial develop rapid sensitive biosensors on-site bacteria. Herein, we developed graphene oxide CRISPR-Cas12a (GO-CRISPR) biosensor bacteria in human serum. In this strategy, single-stranded (ssDNA) FAM probes were quenched with single-layer (GO). Target-activated Cas12a trans-cleavage was utilized degradation ssDNA probes, detaching short GO recovering fluorescent signals. Under optimal conditions, employed our GO-CRISPR system Salmonella Typhimurium (S. Typhimurium) as low 3 × 103 CFU/mL serum, well good specificity toward other competing addition, exhibited excellent S. spiked The offers superior rapidity has potential early resource-limited settings, expediting patients at risk

Language: Английский

Citations

18