Tricking enzymes in living cells: a mechanism-based strategy for design of DNA topoisomerase biosensors
Most activity-based molecular probes are designed to target enzymes that catalyze the breaking of chemical bonds and the conversion of a unimolecular substrate into bimolecular products. However, DNA topoisomerases are a class of enzymes that alter DNA topology without producing any molecular segmen...
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sg-ntu-dr.10356-1613652023-02-28T19:56:09Z Tricking enzymes in living cells: a mechanism-based strategy for design of DNA topoisomerase biosensors Ba, Sai Gao, Guangpeng Li, Tianhu Zhang, Hao School of Physical and Mathematical Sciences Science::Chemistry DNA Topoisomerases Cancer Diagnosis Most activity-based molecular probes are designed to target enzymes that catalyze the breaking of chemical bonds and the conversion of a unimolecular substrate into bimolecular products. However, DNA topoisomerases are a class of enzymes that alter DNA topology without producing any molecular segments during catalysis, which hinders the development of practical methods for diagnosing these key biomarkers in living cells. Here, we established a new strategy for the effective sensing of the expression levels and catalytic activities of topoisomerases in cell-free systems and human cells. Using our newly designed biosensors, we tricked DNA topoisomerases within their catalytic cycles to switch on fluorescence and resume new rounds of catalysis. Considering that human topoisomerases have been widely recognized as biomarkers for multiple cancers and identified as promising targets for several anticancer drugs, we believe that these DNA-based biosensors and our design strategy would greatly benefit the future development of clinical tools for cancer diagnosis and treatment. Published version This work was supported fnancially by the Northwestern Polytechnical University in China through research grant D5000211020. 2022-08-29T08:26:26Z 2022-08-29T08:26:26Z 2021 Journal Article Ba, S., Gao, G., Li, T. & Zhang, H. (2021). Tricking enzymes in living cells: a mechanism-based strategy for design of DNA topoisomerase biosensors. Journal of Nanobiotechnology, 19(1), 407-. https://dx.doi.org/10.1186/s12951-021-01155-1 1477-3155 https://hdl.handle.net/10356/161365 10.1186/s12951-021-01155-1 34876137 2-s2.0-85120909419 1 19 407 en Journal of Nanobiotechnology © The Author(s) 2021. Open Access. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativeco mmons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. application/pdf |
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Science::Chemistry DNA Topoisomerases Cancer Diagnosis Ba, Sai Gao, Guangpeng Li, Tianhu Zhang, Hao Tricking enzymes in living cells: a mechanism-based strategy for design of DNA topoisomerase biosensors |
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Most activity-based molecular probes are designed to target enzymes that catalyze the breaking of chemical bonds and the conversion of a unimolecular substrate into bimolecular products. However, DNA topoisomerases are a class of enzymes that alter DNA topology without producing any molecular segments during catalysis, which hinders the development of practical methods for diagnosing these key biomarkers in living cells. Here, we established a new strategy for the effective sensing of the expression levels and catalytic activities of topoisomerases in cell-free systems and human cells. Using our newly designed biosensors, we tricked DNA topoisomerases within their catalytic cycles to switch on fluorescence and resume new rounds of catalysis. Considering that human topoisomerases have been widely recognized as biomarkers for multiple cancers and identified as promising targets for several anticancer drugs, we believe that these DNA-based biosensors and our design strategy would greatly benefit the future development of clinical tools for cancer diagnosis and treatment. |
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School of Physical and Mathematical Sciences |
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School of Physical and Mathematical Sciences Ba, Sai Gao, Guangpeng Li, Tianhu Zhang, Hao |
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Article |
author |
Ba, Sai Gao, Guangpeng Li, Tianhu Zhang, Hao |
author_sort |
Ba, Sai |
title |
Tricking enzymes in living cells: a mechanism-based strategy for design of DNA topoisomerase biosensors |
title_short |
Tricking enzymes in living cells: a mechanism-based strategy for design of DNA topoisomerase biosensors |
title_full |
Tricking enzymes in living cells: a mechanism-based strategy for design of DNA topoisomerase biosensors |
title_fullStr |
Tricking enzymes in living cells: a mechanism-based strategy for design of DNA topoisomerase biosensors |
title_full_unstemmed |
Tricking enzymes in living cells: a mechanism-based strategy for design of DNA topoisomerase biosensors |
title_sort |
tricking enzymes in living cells: a mechanism-based strategy for design of dna topoisomerase biosensors |
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2022 |
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https://hdl.handle.net/10356/161365 |
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1759854134401433600 |