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A novel ternary heterostructure with dramatic SERS activity for evaluation of PD-L1 expression at the single-cell level
Surface-enhanced Raman scattering (SERS) probes based on a charge transfer (CT) process with high stability and reproducibility are powerful tools under open-air conditions. However, the key problem ahead of practical usage of CT-based SERS technology is how to effectively improve sensitivity. Here,...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6214639/ https://www.ncbi.nlm.nih.gov/pubmed/30406203 http://dx.doi.org/10.1126/sciadv.aau3494 |
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author | Feng, Enduo Zheng, Tingting He, Xiaoxiao Chen, Jinquan Tian, Yang |
author_facet | Feng, Enduo Zheng, Tingting He, Xiaoxiao Chen, Jinquan Tian, Yang |
author_sort | Feng, Enduo |
collection | PubMed |
description | Surface-enhanced Raman scattering (SERS) probes based on a charge transfer (CT) process with high stability and reproducibility are powerful tools under open-air conditions. However, the key problem ahead of practical usage of CT-based SERS technology is how to effectively improve sensitivity. Here, a novel ternary heterostructure SERS substrate, Fe(3)O(4)@GO@TiO(2), with a significant enhancement factor of 8.08 × 10(6) was first synthesized. We found the remarkable enhanced effect of SERS signal to be attributed to the resonance effect of CuPc, CT between GO and TiO(2), and enrichment from a porous TiO(2) shell. In addition, we developed a robust SERS probe with good recyclability under visible light illumination on Fe(3)O(4)@GO@TiO(2) nanocomposites toward ultrasensitive detection of cancer cells down to three cells. We have now successfully applied this probe for in situ quantification and imaging of programmed cell death receptor ligand 1 (PD-L1) on triple-negative breast cancer cell surface at the single-cell level and for monitoring the expression variation of PD-L1 during drug treatment. |
format | Online Article Text |
id | pubmed-6214639 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-62146392018-11-07 A novel ternary heterostructure with dramatic SERS activity for evaluation of PD-L1 expression at the single-cell level Feng, Enduo Zheng, Tingting He, Xiaoxiao Chen, Jinquan Tian, Yang Sci Adv Research Articles Surface-enhanced Raman scattering (SERS) probes based on a charge transfer (CT) process with high stability and reproducibility are powerful tools under open-air conditions. However, the key problem ahead of practical usage of CT-based SERS technology is how to effectively improve sensitivity. Here, a novel ternary heterostructure SERS substrate, Fe(3)O(4)@GO@TiO(2), with a significant enhancement factor of 8.08 × 10(6) was first synthesized. We found the remarkable enhanced effect of SERS signal to be attributed to the resonance effect of CuPc, CT between GO and TiO(2), and enrichment from a porous TiO(2) shell. In addition, we developed a robust SERS probe with good recyclability under visible light illumination on Fe(3)O(4)@GO@TiO(2) nanocomposites toward ultrasensitive detection of cancer cells down to three cells. We have now successfully applied this probe for in situ quantification and imaging of programmed cell death receptor ligand 1 (PD-L1) on triple-negative breast cancer cell surface at the single-cell level and for monitoring the expression variation of PD-L1 during drug treatment. American Association for the Advancement of Science 2018-11-02 /pmc/articles/PMC6214639/ /pubmed/30406203 http://dx.doi.org/10.1126/sciadv.aau3494 Text en Copyright © 2018 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Feng, Enduo Zheng, Tingting He, Xiaoxiao Chen, Jinquan Tian, Yang A novel ternary heterostructure with dramatic SERS activity for evaluation of PD-L1 expression at the single-cell level |
title | A novel ternary heterostructure with dramatic SERS activity for evaluation of PD-L1 expression at the single-cell level |
title_full | A novel ternary heterostructure with dramatic SERS activity for evaluation of PD-L1 expression at the single-cell level |
title_fullStr | A novel ternary heterostructure with dramatic SERS activity for evaluation of PD-L1 expression at the single-cell level |
title_full_unstemmed | A novel ternary heterostructure with dramatic SERS activity for evaluation of PD-L1 expression at the single-cell level |
title_short | A novel ternary heterostructure with dramatic SERS activity for evaluation of PD-L1 expression at the single-cell level |
title_sort | novel ternary heterostructure with dramatic sers activity for evaluation of pd-l1 expression at the single-cell level |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6214639/ https://www.ncbi.nlm.nih.gov/pubmed/30406203 http://dx.doi.org/10.1126/sciadv.aau3494 |
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