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Electron transfer-triggered imaging of EGFR signaling activity
In vivo electron transfer processes are closely related to the activation of signaling pathways, and, thus, affect various life processes. Indeed, the signaling pathway activation of key molecules may be associated with certain diseases. For example, epidermal growth factor receptor (EGFR) activatio...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8807759/ https://www.ncbi.nlm.nih.gov/pubmed/35105871 http://dx.doi.org/10.1038/s41467-022-28213-y |
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author | Tan, Jie Li, Hao Ji, Cailing Zhang, Lei Zhao, Chenxuan Tang, Liming Zhang, Caixin Sun, Zhijun Tan, Weihong Yuan, Quan |
author_facet | Tan, Jie Li, Hao Ji, Cailing Zhang, Lei Zhao, Chenxuan Tang, Liming Zhang, Caixin Sun, Zhijun Tan, Weihong Yuan, Quan |
author_sort | Tan, Jie |
collection | PubMed |
description | In vivo electron transfer processes are closely related to the activation of signaling pathways, and, thus, affect various life processes. Indeed, the signaling pathway activation of key molecules may be associated with certain diseases. For example, epidermal growth factor receptor (EGFR) activation is related to the occurrence and development of tumors. Hence, monitoring the activation of EGFR-related signaling pathways can help reveal the progression of tumor development. However, it is challenging for current detection methods to monitor the activation of specific signaling pathways in complex biochemical reactions. Here we designed a highly sensitive and specific nanoprobe that enables in vivo imaging of electronic transfer over a broad range of spatial and temporal scales. By using the ferrocene-DNA polymer “wire”, the electrons transferred in a biochemical reaction can flow to persistent luminescent nanoparticles and change their electron distribution, thereby altering the optical signal of the particles. This electron transfer-triggered imaging probe enables mapping the activation of EGFR-related signaling pathways in a temporally and spatially precise manner. By offering precise visualization of signaling activity, this approach may offer a general platform not only for understanding molecular mechanisms in various biological processes but also for promoting disease therapies and drug evaluation. |
format | Online Article Text |
id | pubmed-8807759 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-88077592022-02-07 Electron transfer-triggered imaging of EGFR signaling activity Tan, Jie Li, Hao Ji, Cailing Zhang, Lei Zhao, Chenxuan Tang, Liming Zhang, Caixin Sun, Zhijun Tan, Weihong Yuan, Quan Nat Commun Article In vivo electron transfer processes are closely related to the activation of signaling pathways, and, thus, affect various life processes. Indeed, the signaling pathway activation of key molecules may be associated with certain diseases. For example, epidermal growth factor receptor (EGFR) activation is related to the occurrence and development of tumors. Hence, monitoring the activation of EGFR-related signaling pathways can help reveal the progression of tumor development. However, it is challenging for current detection methods to monitor the activation of specific signaling pathways in complex biochemical reactions. Here we designed a highly sensitive and specific nanoprobe that enables in vivo imaging of electronic transfer over a broad range of spatial and temporal scales. By using the ferrocene-DNA polymer “wire”, the electrons transferred in a biochemical reaction can flow to persistent luminescent nanoparticles and change their electron distribution, thereby altering the optical signal of the particles. This electron transfer-triggered imaging probe enables mapping the activation of EGFR-related signaling pathways in a temporally and spatially precise manner. By offering precise visualization of signaling activity, this approach may offer a general platform not only for understanding molecular mechanisms in various biological processes but also for promoting disease therapies and drug evaluation. Nature Publishing Group UK 2022-02-01 /pmc/articles/PMC8807759/ /pubmed/35105871 http://dx.doi.org/10.1038/s41467-022-28213-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Tan, Jie Li, Hao Ji, Cailing Zhang, Lei Zhao, Chenxuan Tang, Liming Zhang, Caixin Sun, Zhijun Tan, Weihong Yuan, Quan Electron transfer-triggered imaging of EGFR signaling activity |
title | Electron transfer-triggered imaging of EGFR signaling activity |
title_full | Electron transfer-triggered imaging of EGFR signaling activity |
title_fullStr | Electron transfer-triggered imaging of EGFR signaling activity |
title_full_unstemmed | Electron transfer-triggered imaging of EGFR signaling activity |
title_short | Electron transfer-triggered imaging of EGFR signaling activity |
title_sort | electron transfer-triggered imaging of egfr signaling activity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8807759/ https://www.ncbi.nlm.nih.gov/pubmed/35105871 http://dx.doi.org/10.1038/s41467-022-28213-y |
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