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Ultrasensitive monitoring of mercury(II) (Hg) in environmental and biological systems is highly desirable due to the fact that this heavy metal ion is a ubiquitous pollutant worldwide. Despite the existence of numerous readily-available techniques for Hg-detection, optical probe-based fluorescence tracking stands out, as this powerful tool can offer the distinct advantages of real-time, noninvasive and particularly in vivo monitoring. Herein, a novel hemicyanine-based fluorescent probe (namely HDS-Hg) with an enhanced turn-on near-infrared (NIR) sensing of fluorescence response upon binding with Hg (λ/λ = 700 nm/765 nm) was constructed, which featured a rapid response, low detection limit, wide pH-tolerance, high sensitivity and selectivity as well as favorable mitochondria-targeting ability. Probe HDS-Hg worked well in monitoring of Hg in environmental water samples, herbs, seafoods and living cells. Notably, HDS-Hg could serve as the first fluorescent probe that can visualize the dynamic fluctuations of Hg levels within tobacco seedling leaves. With the aid of HDS-Hg, real-time monitoring of the Hg-induced liver injury in a chronic mercury poisoning mouse model was also achieved. Undoubtedly, the presented work not only provides a robust imaging tool for detecting Hg in complex environmental and in vivo biological samples, but most importantly it offers critical insights into chronic mercury poisoning.
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http://dx.doi.org/10.1016/j.jhazmat.2025.139462 | DOI Listing |
Mikrochim Acta
September 2025
Pharmaceutical Analysis Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Salmonella Typhimurium (S. Typhimurium) is one of the most common food-borne diseases, highlighted as the top food-borne bacterial pathogen in the world with a low infectious dose (1 CFU) and high mortality rate. It is commonly associated with numerous foods such as dairy products, protein sources (multiple types of meat, poultry, and eggs), and bakery products.
View Article and Find Full Text PDFPhotochem Photobiol Sci
September 2025
Department of Genetics and Plant Breeding, C. P. College of Agriculture, S. D. Agricultural University, Sardarkrushinagar, 385506, India.
The electromobility shift assay (EMSA) is a popular and productive molecular biology tool for studying protein-nucleic acid interactions. EMSA is a technique applied to the revelation of the binding dynamics of proteins, like transcription factors, to DNA or RNA. There are ample essential phases in the technique.
View Article and Find Full Text PDFLuminescence
September 2025
Department of Chemistry, Institute of Science, Banaras Hindu University, Varanasi, Uttar Pradesh, India.
A triphenyl-imidazole end-capped donor-acceptor type potential molecular probe 3 has been designed and synthesized. Probe 3 upon interaction with different classes of metal ions/anions and NPPs displayed high selectivity with CN anion (LOD = 20.42 nM) through fluorescence "turn-Off" response and a naked-eye sensitive visible color change.
View Article and Find Full Text PDFNucleic Acids Res
September 2025
Biomolecular Sciences Institute, Florida International University, Miami, FL 33199, United States.
Supercoiled (Sc) circular DNA, such as plasmids, are essential in molecular biology and hold strong therapeutic potential. However, they are typically produced in Escherichia coli, resulting in bacterial methylations, unnecessary sequences, and contaminants that hinder certain applications including clinical uses. These limitations could be avoided by synthesizing plasmids entirely in vitro, but synthesizing high-purity Sc circular DNA biochemically remains a significant technical challenge.
View Article and Find Full Text PDFNucleic Acids Res
September 2025
Department of Chemistry and Henry Eyring Center for Cell and Genome Science, University of Utah, Salt Lake City, UT 84112, United States.
Glycine is an important metabolite and cell signal in diverse organisms, yet tools to visualize intracellular glycine dynamics have not been developed. In this study, diverse and bright RNA-based glycine biosensors were developed by fusing the architecturally complex glycine riboswitch with Broccoli class fluorogenic aptamers. The brightest sensor with the highest activation, glyS, and its two-dye ratiometric counterpart, Pepper-glyS, allowed for visualization of a drug-induced accumulation of endogenous glycine in live Escherichia colicells.
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