Abstract:Analytical performance and efficiency are two pivotal issues for developing an on-site and real-time aptasensor for cadmium (Cd2+) determination. However, suffering from redundant preparations, fabrications, and incubation, most of them fail to well satisfy the requirements. In this work, we found that fluorescence intensity of 6-carboxyfluorescein(FAM)-labeled aptamer (FAM-aptamer) could be remarkably amplified by 3-(N-morpholino)propane sulfonic acid (MOPS), then fell proportionally as Cd2+ concentration int… Show more
“…The investigative enzymes like CAT, POD, APX and SOD perform an essential function in the metabolic responses of environmental stress function in crop [ [53] , [64] , [71] ]. Liu et al [ 72 ] reported that the increased in the activities of SOD and CAT in Si treated plants present enhanced modification of O to H 2 O 2 as similar to Si treatment in Refs. [ 73 , 74 ].…”
“…The investigative enzymes like CAT, POD, APX and SOD perform an essential function in the metabolic responses of environmental stress function in crop [ [53] , [64] , [71] ]. Liu et al [ 72 ] reported that the increased in the activities of SOD and CAT in Si treated plants present enhanced modification of O to H 2 O 2 as similar to Si treatment in Refs. [ 73 , 74 ].…”
“…The quenching efficiency was determined by the formula ( F 1 − F 0 )/ F 1 , where F 1 and F 0 are the fluorescence signals of ATP aptamers before and after adding GO. 31 The signal-to-noise ratio (SNR) was determined by the formula SNR = F / F 0 , where F represents the recovered fluorescence intensity and F 0 is the quenched fluorescence intensity before adding the target compounds. 32 The correlation between GO concentration and quenching efficiency was obtained by recording the plateau quenching at different GO concentrations.…”
A modifiable droplet graphene oxide (GO) aptasensor has been developed for low-background detection of various target compounds with enhanced signal-to-noise ratios for synthetic biology applications.
“…Fluorescence quenching efficiency was calculated using the formula below [ 47 ]: where F PC is the emission intensity of SQ-122 PC, and F dye is the emission intensity of the SQ-122 dye at the same concentration in H 2 O (30%).…”
Chymotrypsin, a crucial enzyme in human digestion, catalyzes the breakdown of milk proteins, underscoring its significance in both health diagnostics and dairy quality assurance. Addressing the critical need for rapid, cost-effective detection methods, we introduce a groundbreaking approach utilizing far-red technology and HOMO-Förster resonance energy transfer (FRET). Our novel probe, SQ-122 PC, features a unique molecular design that includes a squaraine dye (SQ), a peptide linker, and SQ moieties synthesized through solid-phase peptide synthesis. Demonstrating a remarkable quenching efficiency of 93.75% in a tailored H2O:DMSO (7:3) solvent system, our probe exhibits absorption and emission properties within the far-red spectrum, with an unprecedented detection limit of 0.130 nM. Importantly, our method offers unparalleled selectivity towards chymotrypsin, ensuring robust and accurate enzyme detection. This pioneering work underscores the immense potential of far-red-based homo-FRET systems in enabling the sensitive and specific detection of chymotrypsin enzyme activity. By bridging the gap between cutting-edge technology and biomedical diagnostics, our findings herald a new era of enzyme sensing, promising transformative advancements in disease diagnosis and dairy quality control.
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