Food Control, Journal Year: 2024, Volume and Issue: unknown, P. 111049 - 111049
Published: Nov. 1, 2024
Language: Английский
Food Control, Journal Year: 2024, Volume and Issue: unknown, P. 111049 - 111049
Published: Nov. 1, 2024
Language: Английский
EBioMedicine, Journal Year: 2025, Volume and Issue: 112, P. 105564 - 105564
Published: Jan. 24, 2025
Language: Английский
Citations
1Biosensors and Bioelectronics, Journal Year: 2025, Volume and Issue: 276, P. 117256 - 117256
Published: Feb. 13, 2025
Language: Английский
Citations
1Trends in biotechnology, Journal Year: 2024, Volume and Issue: unknown
Published: Aug. 1, 2024
Language: Английский
Citations
4Analytical Chemistry, Journal Year: 2025, Volume and Issue: unknown
Published: Feb. 9, 2025
Strategies for the rapid detection of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) are critically needed due to conventional methods' limitations: narrow range, virus mutation-induced failure, time-consuming, and complex operations. Herein, we propose a method utilizing CuInP2S6 nanosheet probes Bio-Layer Interferometry (BLI) technology (5–10 min), noninvasive, broad-spectrum SARS-CoV-2 spike receptor binding domain (RBD) in human saliva. The nanoprobe exhibits higher affinity RBD compared most saliva proteins, allowing it be immobilized on BLI sensors easier protein elution. An eluent buffer containing Tween-20 salts was employed separate salivary proteins while retaining probes. This system can detect across broad spectrum low limit 25 ng/mL (S/N = 3) less than 10 min. To validate this system, experiments with pseudoviruses showed accurate identification RBD. Molecular dynamics simulations elucidated mechanism selective In conclusion, conceptual study based an situ strategy inorganic nanoprobes alongside techniques convenient, its variants. is anticipated inspire design implementation pathogens future.
Language: Английский
Citations
0Analytical Chemistry, Journal Year: 2025, Volume and Issue: unknown
Published: March 11, 2025
CRISPR-Cas systems represent a highly programmable and precise nucleic acid-targeting platform, which has been strategically engineered as versatile toolkit for biosensing bioimaging applications. Nevertheless, their analytical performance is constrained by inherent functional activity limitations of natural CRISPR/Cas systems, underscoring the critical role molecular engineering in enhancing capabilities. This review comprehensively examines recent advancements ribonucleoproteins (RNPs) to enhance capabilities advanced detection cellular imaging. We explore innovative strategies developing enhanced RNPs, including Cas protein through mutagenesis fusion techniques, guide RNA via chemical structural modifications. Furthermore, we evaluate these RNPs' applications sensitive biomarker live-cell genomic DNA monitoring, while analyzing current challenges prospective developments RNP bioimaging.
Language: Английский
Citations
0Biosensors and Bioelectronics, Journal Year: 2025, Volume and Issue: unknown, P. 117458 - 117458
Published: April 1, 2025
Language: Английский
Citations
0Advances in Colloid and Interface Science, Journal Year: 2024, Volume and Issue: 332, P. 103276 - 103276
Published: Aug. 12, 2024
Language: Английский
Citations
3Sensing and Bio-Sensing Research, Journal Year: 2025, Volume and Issue: unknown, P. 100736 - 100736
Published: Jan. 1, 2025
Language: Английский
Citations
0ACS Sensors, Journal Year: 2025, Volume and Issue: 10(1), P. 1 - 3
Published: Jan. 24, 2025
Language: Английский
Citations
0Sensing and Bio-Sensing Research, Journal Year: 2025, Volume and Issue: 48, P. 100797 - 100797
Published: April 29, 2025
Language: Английский
Citations
0