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Label-free and Non-destruction Determination of Single- and Double-Strand DNA based on Quantum Weak Measurement

The process of unwinding and renaturation of DNA has been widely used in studies of nucleotide sequence organization. Compared with traditional methods for DNA unwinding and renaturation, the label-free and non-destruction detection technology is significant and desiderated. We realized an optical s...

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Autores principales: Guan, Tian, Yang, Yuxuan, Zhang, Qianwen, He, Yonghong, Xu, Naihan, Li, Dongmei, Shi, Lixuan, Xu, Yang, Wang, Xiangnan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6374449/
https://www.ncbi.nlm.nih.gov/pubmed/30760805
http://dx.doi.org/10.1038/s41598-018-38454-x
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author Guan, Tian
Yang, Yuxuan
Zhang, Qianwen
He, Yonghong
Xu, Naihan
Li, Dongmei
Shi, Lixuan
Xu, Yang
Wang, Xiangnan
author_facet Guan, Tian
Yang, Yuxuan
Zhang, Qianwen
He, Yonghong
Xu, Naihan
Li, Dongmei
Shi, Lixuan
Xu, Yang
Wang, Xiangnan
author_sort Guan, Tian
collection PubMed
description The process of unwinding and renaturation of DNA has been widely used in studies of nucleotide sequence organization. Compared with traditional methods for DNA unwinding and renaturation, the label-free and non-destruction detection technology is significant and desiderated. We realized an optical system based on optical rotation via weak measurement for detection of single- and double-strand state of DNA. The optical rotation, which was induced by the status change of single and double DNA strands, was exploited to modulate the preselected polarization of a weak measurement system. With this modulation, the optical rotation caused by the separation of DNA strands can be determined through the center wavelength shift of the output spectrum. By monitoring the wavelength shift in real time, the separation processes of the DNAs with different base ratio (25% and 70%) and length (4nt and 40nt), and DNAs with three terminally modified cholesterol molecules were experimentally explored in varied pH and temperature conditions. In addition, the detection limit of the DNA concentration was obtained to be 5 × 10(−6) mol/L. Our work based on optical rotation detection of single- and double-strand DNA exhibits the unique advantages of real-time monitoring, label-free, non-destruction and simplicity.
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spelling pubmed-63744492019-02-19 Label-free and Non-destruction Determination of Single- and Double-Strand DNA based on Quantum Weak Measurement Guan, Tian Yang, Yuxuan Zhang, Qianwen He, Yonghong Xu, Naihan Li, Dongmei Shi, Lixuan Xu, Yang Wang, Xiangnan Sci Rep Article The process of unwinding and renaturation of DNA has been widely used in studies of nucleotide sequence organization. Compared with traditional methods for DNA unwinding and renaturation, the label-free and non-destruction detection technology is significant and desiderated. We realized an optical system based on optical rotation via weak measurement for detection of single- and double-strand state of DNA. The optical rotation, which was induced by the status change of single and double DNA strands, was exploited to modulate the preselected polarization of a weak measurement system. With this modulation, the optical rotation caused by the separation of DNA strands can be determined through the center wavelength shift of the output spectrum. By monitoring the wavelength shift in real time, the separation processes of the DNAs with different base ratio (25% and 70%) and length (4nt and 40nt), and DNAs with three terminally modified cholesterol molecules were experimentally explored in varied pH and temperature conditions. In addition, the detection limit of the DNA concentration was obtained to be 5 × 10(−6) mol/L. Our work based on optical rotation detection of single- and double-strand DNA exhibits the unique advantages of real-time monitoring, label-free, non-destruction and simplicity. Nature Publishing Group UK 2019-02-13 /pmc/articles/PMC6374449/ /pubmed/30760805 http://dx.doi.org/10.1038/s41598-018-38454-x Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Guan, Tian
Yang, Yuxuan
Zhang, Qianwen
He, Yonghong
Xu, Naihan
Li, Dongmei
Shi, Lixuan
Xu, Yang
Wang, Xiangnan
Label-free and Non-destruction Determination of Single- and Double-Strand DNA based on Quantum Weak Measurement
title Label-free and Non-destruction Determination of Single- and Double-Strand DNA based on Quantum Weak Measurement
title_full Label-free and Non-destruction Determination of Single- and Double-Strand DNA based on Quantum Weak Measurement
title_fullStr Label-free and Non-destruction Determination of Single- and Double-Strand DNA based on Quantum Weak Measurement
title_full_unstemmed Label-free and Non-destruction Determination of Single- and Double-Strand DNA based on Quantum Weak Measurement
title_short Label-free and Non-destruction Determination of Single- and Double-Strand DNA based on Quantum Weak Measurement
title_sort label-free and non-destruction determination of single- and double-strand dna based on quantum weak measurement
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6374449/
https://www.ncbi.nlm.nih.gov/pubmed/30760805
http://dx.doi.org/10.1038/s41598-018-38454-x
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