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Triggering molecular assembly at the mesoscale for advanced Raman detection of proteins in liquid
An advanced optofluidic system for protein detection based on Raman signal amplification via dewetting and molecular gathering within temporary mesoscale assemblies is presented. The evaporation of a microliter volume of protein solution deposited in a circular microwell precisely follows an outward...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5773671/ https://www.ncbi.nlm.nih.gov/pubmed/29348509 http://dx.doi.org/10.1038/s41598-018-19558-w |
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author | Banchelli, Martina de Angelis, Marella D’Andrea, Cristiano Pini, Roberto Matteini, Paolo |
author_facet | Banchelli, Martina de Angelis, Marella D’Andrea, Cristiano Pini, Roberto Matteini, Paolo |
author_sort | Banchelli, Martina |
collection | PubMed |
description | An advanced optofluidic system for protein detection based on Raman signal amplification via dewetting and molecular gathering within temporary mesoscale assemblies is presented. The evaporation of a microliter volume of protein solution deposited in a circular microwell precisely follows an outward-receding geometry. Herein the combination of liquid withdrawal with intermolecular interactions induces the formation of self-assembled molecular domains at the solid-liquid interface. Through proper control of the evaporation rate, amplitude of the assemblies and time for spectral collection at the liquid edge are extensively raised, resulting in a local enhancement and refinement of the Raman response, respectively. Further signal amplification is obtained by taking advantage of the intense local electromagnetic fields generated upon adding a plasmonic coating to the microwell. Major advantages of this optofluidic method lie in the obtainment of high-quality, high-sensitivity Raman spectra with detection limit down to sub-micromolar values. Peculiarly, the assembled proteins in the liquid edge region maintain their native-like state without displaying spectral changes usually occurring when dried drop deposits are considered. |
format | Online Article Text |
id | pubmed-5773671 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57736712018-01-26 Triggering molecular assembly at the mesoscale for advanced Raman detection of proteins in liquid Banchelli, Martina de Angelis, Marella D’Andrea, Cristiano Pini, Roberto Matteini, Paolo Sci Rep Article An advanced optofluidic system for protein detection based on Raman signal amplification via dewetting and molecular gathering within temporary mesoscale assemblies is presented. The evaporation of a microliter volume of protein solution deposited in a circular microwell precisely follows an outward-receding geometry. Herein the combination of liquid withdrawal with intermolecular interactions induces the formation of self-assembled molecular domains at the solid-liquid interface. Through proper control of the evaporation rate, amplitude of the assemblies and time for spectral collection at the liquid edge are extensively raised, resulting in a local enhancement and refinement of the Raman response, respectively. Further signal amplification is obtained by taking advantage of the intense local electromagnetic fields generated upon adding a plasmonic coating to the microwell. Major advantages of this optofluidic method lie in the obtainment of high-quality, high-sensitivity Raman spectra with detection limit down to sub-micromolar values. Peculiarly, the assembled proteins in the liquid edge region maintain their native-like state without displaying spectral changes usually occurring when dried drop deposits are considered. Nature Publishing Group UK 2018-01-18 /pmc/articles/PMC5773671/ /pubmed/29348509 http://dx.doi.org/10.1038/s41598-018-19558-w Text en © The Author(s) 2018 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 Banchelli, Martina de Angelis, Marella D’Andrea, Cristiano Pini, Roberto Matteini, Paolo Triggering molecular assembly at the mesoscale for advanced Raman detection of proteins in liquid |
title | Triggering molecular assembly at the mesoscale for advanced Raman detection of proteins in liquid |
title_full | Triggering molecular assembly at the mesoscale for advanced Raman detection of proteins in liquid |
title_fullStr | Triggering molecular assembly at the mesoscale for advanced Raman detection of proteins in liquid |
title_full_unstemmed | Triggering molecular assembly at the mesoscale for advanced Raman detection of proteins in liquid |
title_short | Triggering molecular assembly at the mesoscale for advanced Raman detection of proteins in liquid |
title_sort | triggering molecular assembly at the mesoscale for advanced raman detection of proteins in liquid |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5773671/ https://www.ncbi.nlm.nih.gov/pubmed/29348509 http://dx.doi.org/10.1038/s41598-018-19558-w |
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