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Updated: Jan 26, 2026

In vitro Reconstitution of the Active T. castaneum Telomerase
Published on: July 14, 2011
A conformational switch-based fluorescent biosensor for homogeneous detection of telomerase activity
Ying Zhou1, Shujuan Shen1, Choiwan Lau1
1School of Pharmacy, Fudan University, 826 Zhangheng Road, Shanghai 201203, China.
Abstract:
As a universal tumor biomarker, research on the activity and inhibition of telomerase is of great importance for cancer diagnosis and therapy. Herein, we demonstrate the conformational switch-based fluorescence detection of telomerase activity using a redesigned RNA aptamer Spinach. Briefly, the original Spinach aptamer was extended at its 5' end and folded into an inactive conformation, where association with the small molecule fluorophore, 5-difluoro-4-hydroxybenzylidene imidazolinone (DFHBI) was prevented. Only in the presence of telomerase, (TTAGGG)n repeats were added to the 3' end of the telomerase substrate primer, and the elongation products hybridized with inactive Spinach molecules, triggering its conformational switch and refolding it into the active, DFHBI-binding conformation. Moreover, the fluorescence signal was further amplified through a target recycling circuit, where Ribonuclease H (RNase H) specifically hydrolyzed the phosphodiester bonds of RNA in the DNA-RNA hybrid. The released telomere products could then hybridize to new inactive Spinach molecules and initiate multiple amplification cycles. The proposed fluorescent biosensor presented great performance for telomerase activity detection from 100 to 5 × 104 Hela cells with a detection limit of 100 cells. Besides, this new assay offers a good biosensing platform for differentiation of cancer cell lines from normal cell line and evaluation the inhibition efficiency of telomere-binding ligand, which is of great importance for telomerase-related cancer diagnosis and therapy.
Insights
This study presents a new fluorescence biosensor for detecting telomerase activity. The assay uses a conformational switch in an RNA aptamer (Spinach) for sensitive cancer cell detection and evaluation of telomerase inhibition.
Area of Science:
- Biochemistry
- Molecular Biology
- Biomedical Engineering
Background:
- Telomerase is a crucial biomarker for cancer diagnosis and therapy due to its universal presence in tumors.
- Existing methods for telomerase detection require complex procedures and lack sensitivity for early diagnosis.
- Developing novel, sensitive, and efficient biosensors for telomerase activity is essential for advancing cancer research.
Purpose of the Study:
- To develop a conformational switch-based fluorescence biosensor for sensitive detection of telomerase activity.
- To utilize a redesigned RNA aptamer (Spinach) for enhanced fluorescence signaling.
- To establish a platform for cancer cell line differentiation and evaluation of telomerase inhibition.
Main Methods:
- A modified Spinach RNA aptamer was engineered to exist in an inactive conformation, preventing fluorophore binding.
- Telomerase activity, by adding telomere repeats, triggers a conformational switch in the aptamer, enabling DFHBI binding and fluorescence.
- A target recycling circuit involving Ribonuclease H (RNase H) was implemented for signal amplification.
Main Results:
- The biosensor demonstrated high performance in detecting telomerase activity across a range of 100 to 5 x 10^4 HeLa cells.
- A low detection limit of 100 cells was achieved, indicating significant sensitivity.
- The assay successfully differentiated cancer cell lines from normal cell lines and evaluated telomere-binding ligand inhibition.
Conclusions:
- The developed conformational switch-based fluorescent biosensor offers a sensitive and efficient method for telomerase activity detection.
- This assay serves as a valuable platform for cancer diagnosis, differentiation of cell lines, and assessment of therapeutic efficacy.
- The findings hold significant implications for advancing telomerase-targeted cancer therapy and diagnostics.
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