A molecular beacon biosensor for viral RNA detection based on HyCaSD strategy
In the present study, a molecular beacon biosensor was developed to enable efficient detection of the viral RNAs using a previously described HyCaSD platform. The HyCaSD molecular beacon probes were labeled with the Cy5 and BHQ3 at each end of the hairpin probes. The fluorescent signal was detected...
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th-mahidol.836322023-06-18T23:45:48Z A molecular beacon biosensor for viral RNA detection based on HyCaSD strategy Saisuk W. Mahidol University Biochemistry, Genetics and Molecular Biology In the present study, a molecular beacon biosensor was developed to enable efficient detection of the viral RNAs using a previously described HyCaSD platform. The HyCaSD molecular beacon probes were labeled with the Cy5 and BHQ3 at each end of the hairpin probes. The fluorescent signal was detected immediately only when the molecular beacon probes specifically hybridized to the target sequence and unfolded their hairpin structures. This combination greatly improved the sensitivity with LOD of 100 copy equivalents per reaction (around 20-fold greater than the original HyCaSD). In addition, our MB-based HyCaSD demonstrated a single-step, single-tube and actual-time RNA detection procedure, thereby bringing it a major step closer to point-of-care diagnostic applications for viral infectious diseases. 2023-06-18T16:45:48Z 2023-06-18T16:45:48Z 2022-08-15 Article Analytica Chimica Acta Vol.1221 (2022) 10.1016/j.aca.2022.340134 18734324 00032670 35934369 2-s2.0-85133706132 https://repository.li.mahidol.ac.th/handle/123456789/83632 SCOPUS |
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Biochemistry, Genetics and Molecular Biology Saisuk W. A molecular beacon biosensor for viral RNA detection based on HyCaSD strategy |
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In the present study, a molecular beacon biosensor was developed to enable efficient detection of the viral RNAs using a previously described HyCaSD platform. The HyCaSD molecular beacon probes were labeled with the Cy5 and BHQ3 at each end of the hairpin probes. The fluorescent signal was detected immediately only when the molecular beacon probes specifically hybridized to the target sequence and unfolded their hairpin structures. This combination greatly improved the sensitivity with LOD of 100 copy equivalents per reaction (around 20-fold greater than the original HyCaSD). In addition, our MB-based HyCaSD demonstrated a single-step, single-tube and actual-time RNA detection procedure, thereby bringing it a major step closer to point-of-care diagnostic applications for viral infectious diseases. |
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Mahidol University |
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Mahidol University Saisuk W. |
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Saisuk W. |
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Saisuk W. |
title |
A molecular beacon biosensor for viral RNA detection based on HyCaSD strategy |
title_short |
A molecular beacon biosensor for viral RNA detection based on HyCaSD strategy |
title_full |
A molecular beacon biosensor for viral RNA detection based on HyCaSD strategy |
title_fullStr |
A molecular beacon biosensor for viral RNA detection based on HyCaSD strategy |
title_full_unstemmed |
A molecular beacon biosensor for viral RNA detection based on HyCaSD strategy |
title_sort |
molecular beacon biosensor for viral rna detection based on hycasd strategy |
publishDate |
2023 |
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https://repository.li.mahidol.ac.th/handle/123456789/83632 |
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1781414384123248640 |