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The Preparation of CuInS(2)-ZnS-Glutathione Quantum Dots and Their Application on the Sensitive Determination of Cytochrome c and Imaging of HeLa Cells
[Image: see text] Cytochrome c (Cyt c), one of the most significant proteins acting as an electron transporter, plays an important role during the transferring process of the energy in cells. Apoptosis, one of the major forms of cell death, has been associated with various physiological regularity a...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8280654/ https://www.ncbi.nlm.nih.gov/pubmed/34278136 http://dx.doi.org/10.1021/acsomega.1c01983 |
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author | An, Xiangyang Zhang, Yuemei Wang, Jing Kong, De-ming He, Xi-wen Chen, Langxing Zhang, Yukui |
author_facet | An, Xiangyang Zhang, Yuemei Wang, Jing Kong, De-ming He, Xi-wen Chen, Langxing Zhang, Yukui |
author_sort | An, Xiangyang |
collection | PubMed |
description | [Image: see text] Cytochrome c (Cyt c), one of the most significant proteins acting as an electron transporter, plays an important role during the transferring process of the energy in cells. Apoptosis, one of the major forms of cell death, has been associated with various physiological regularity and pathological mechanisms. It was found that Cyt c can be released from mitochondria to cytosol under different pathological conditions, triggering subsequent cell apoptosis. Herein, we developed a fluorescence nanoprobe based on negatively charged CuInS(2)-ZnS-GSH quantum dots (QDs) for the sensitive determination of Cyt c. CuInS(2)-ZnS-GSH QDs with high photochemical stability and favorable hydrophilicity were prepared by a simple hot reflux method and emit a bright orange-red light. The electron-deficient heme group in Cyt c is affiliated with the electron-rich CuInS(2)-ZnS-GSH QDs through the photo-induced electron transfer process, resulting in a large decrease in fluorescence intensity of QDs. A good linearity for concentration of Cyt c in the range of 0.01–7 μmol L(–1) is obtained, and the detection limit of Cyt c is as low as 1.1 nM. The performance on the detection of Cyt c in spiked human serum and fetal bovine serum samples showed good recoveries from 85.5% to 95.0%. Furthermore, CuInS(2)-ZnS-GSH QDs were applied for the intracellular imaging in HeLa cells showing an extremely lower toxicity and excellent biocompatibility. |
format | Online Article Text |
id | pubmed-8280654 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-82806542021-07-16 The Preparation of CuInS(2)-ZnS-Glutathione Quantum Dots and Their Application on the Sensitive Determination of Cytochrome c and Imaging of HeLa Cells An, Xiangyang Zhang, Yuemei Wang, Jing Kong, De-ming He, Xi-wen Chen, Langxing Zhang, Yukui ACS Omega [Image: see text] Cytochrome c (Cyt c), one of the most significant proteins acting as an electron transporter, plays an important role during the transferring process of the energy in cells. Apoptosis, one of the major forms of cell death, has been associated with various physiological regularity and pathological mechanisms. It was found that Cyt c can be released from mitochondria to cytosol under different pathological conditions, triggering subsequent cell apoptosis. Herein, we developed a fluorescence nanoprobe based on negatively charged CuInS(2)-ZnS-GSH quantum dots (QDs) for the sensitive determination of Cyt c. CuInS(2)-ZnS-GSH QDs with high photochemical stability and favorable hydrophilicity were prepared by a simple hot reflux method and emit a bright orange-red light. The electron-deficient heme group in Cyt c is affiliated with the electron-rich CuInS(2)-ZnS-GSH QDs through the photo-induced electron transfer process, resulting in a large decrease in fluorescence intensity of QDs. A good linearity for concentration of Cyt c in the range of 0.01–7 μmol L(–1) is obtained, and the detection limit of Cyt c is as low as 1.1 nM. The performance on the detection of Cyt c in spiked human serum and fetal bovine serum samples showed good recoveries from 85.5% to 95.0%. Furthermore, CuInS(2)-ZnS-GSH QDs were applied for the intracellular imaging in HeLa cells showing an extremely lower toxicity and excellent biocompatibility. American Chemical Society 2021-06-30 /pmc/articles/PMC8280654/ /pubmed/34278136 http://dx.doi.org/10.1021/acsomega.1c01983 Text en © 2021 The Authors. Published by American Chemical Society Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | An, Xiangyang Zhang, Yuemei Wang, Jing Kong, De-ming He, Xi-wen Chen, Langxing Zhang, Yukui The Preparation of CuInS(2)-ZnS-Glutathione Quantum Dots and Their Application on the Sensitive Determination of Cytochrome c and Imaging of HeLa Cells |
title | The Preparation of CuInS(2)-ZnS-Glutathione
Quantum Dots and Their Application on the Sensitive Determination
of Cytochrome c and Imaging of HeLa Cells |
title_full | The Preparation of CuInS(2)-ZnS-Glutathione
Quantum Dots and Their Application on the Sensitive Determination
of Cytochrome c and Imaging of HeLa Cells |
title_fullStr | The Preparation of CuInS(2)-ZnS-Glutathione
Quantum Dots and Their Application on the Sensitive Determination
of Cytochrome c and Imaging of HeLa Cells |
title_full_unstemmed | The Preparation of CuInS(2)-ZnS-Glutathione
Quantum Dots and Their Application on the Sensitive Determination
of Cytochrome c and Imaging of HeLa Cells |
title_short | The Preparation of CuInS(2)-ZnS-Glutathione
Quantum Dots and Their Application on the Sensitive Determination
of Cytochrome c and Imaging of HeLa Cells |
title_sort | preparation of cuins(2)-zns-glutathione
quantum dots and their application on the sensitive determination
of cytochrome c and imaging of hela cells |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8280654/ https://www.ncbi.nlm.nih.gov/pubmed/34278136 http://dx.doi.org/10.1021/acsomega.1c01983 |
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