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The self-quenching fluorogenic probe facilitates precise identification of LAMP (loop-mediated isothermal amplification) amplicons, unaffected by non-specific products resulting from primer dimers. However, low quenching efficiency by surrounding nucleobases leads to high background signal, posing significant challenges for visual inspection with the naked eye. The present study aims to identify an oligonucleotide sequence that is complementary to the self-quenching fluorogenic probe, and to employ the fluorescence super-quenching mechanism of double-stranded DNA to establish a visualization system for the LAMP assay. The results indicated that the incorporation of a sequence fully complementary to the probe could significantly reduce the system's background fluorescence ( < 0.05). When the melting temperature exceeds room temperature, truncating the complementary sequence from the 3' end does not compromise the probe's quenching efficiency. The LAMP visualization system, using a 10-13-base complementary sequence of the loop primer-based probe, could effectively minimize background fluorescence and yield straightforward visual results post-reaction. Applied to rainbow trout and Atlantic salmon detection, the system detected 1 pg DNA in a closed-tube format. In conclusion, a suitable complementary sequence can reduce the background fluorescence of the self-quenching fluorogenic probe. Employing this sequence alongside the self-quenching fluorogenic probe to develop a low-background fluorescence LAMP system demonstrates great potential for successful visual detection and holds considerable promotional merit.
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http://dx.doi.org/10.3390/foods13233816 | DOI Listing |
Anal Chim Acta
September 2025
Institute of Drug Metabolism and Pharmaceutical Analysis, Research Center for Clinical Pharmacy, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, 310058, China; Key Laboratory of Molecular Pharmacology and Drug Evaluation (Yantai University), Ministry of Education, Yantai Universit
Background: Human β-galactosidase (β-gal) is a lysosomal enzyme responsible for the hydrolysis of glycoconjugates, which is overexpressed in primary ovarian cancers and regarded as a biomarker. Therefore, it is of great importance to develop fluorescent probes activatable by endogenous β-gal with strong signal-to-background contrast to facilitate ovarian cancer diagnosis. Many of the available probes suffer from small Stokes shifts, poor cellular permeability, easy diffusion away from living cells, and self-quenching when accumulated inside the lysosome, asking for the development of new turn-on probes suitable for non-invasive imaging with living cells.
View Article and Find Full Text PDFFoods
November 2024
College of Light Industry and Food Engineering, Nanjing Forestry University, Nanjing 210037, China.
The self-quenching fluorogenic probe facilitates precise identification of LAMP (loop-mediated isothermal amplification) amplicons, unaffected by non-specific products resulting from primer dimers. However, low quenching efficiency by surrounding nucleobases leads to high background signal, posing significant challenges for visual inspection with the naked eye. The present study aims to identify an oligonucleotide sequence that is complementary to the self-quenching fluorogenic probe, and to employ the fluorescence super-quenching mechanism of double-stranded DNA to establish a visualization system for the LAMP assay.
View Article and Find Full Text PDFFood Chem
May 2024
College of Food Science and Light Industry, Nanjing Tech University, Nanjing 211800, China. Electronic address:
Single-modified fluorogenic primer (Sfp) enables accurate identification of LAMP amplicons without being affected by non-specific products. However, the fluorescence self-quenching by nucleobases for Sfp is generally of low efficiency, and the high background signal makes it a great challenge to achieve visual inspection with naked eyes. In the present study, the oligonucleotide (Ao) complementary to Sfp was designed, which would hybridize to Sfp and dramatically heighten the quenching effect, leading to a low background signal in negative reaction.
View Article and Find Full Text PDFChem Sci
April 2023
Institut für Chemie, Humboldt-Universität zu Berlin 12489 Berlin Germany
Efficient fluorogenic hybridization probes combine high brightness and specificity of fluorescence signaling with large turn-on of fluorescence. Herein, we present an approach to enhance signaling by combining two identical fluorescence base surrogates in FIT probes. Provided there is a suitable positioning of dyes, target-bound FIT probes emit brighter than mono dye probes, while dye-dye contact in the single stranded state provides opportunities for decreasing background fluorescence.
View Article and Find Full Text PDFNat Methods
May 2022
Department of Cell Biology, Yale University, New Haven, CT, USA.
DNA-based points accumulation for imaging in nanoscale topography (DNA-PAINT) is a powerful super-resolution microscopy method that can acquire high-fidelity images at nanometer resolution. It suffers, however, from high background and slow imaging speed, both of which can be attributed to the presence of unbound fluorophores in solution. Here we present two-color fluorogenic DNA-PAINT, which uses improved imager probe and docking strand designs to solve these problems.
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