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Nanowaveguide-illuminated fluorescence correlation spectroscopy for single molecule studies
Fluorescence Correlation Spectroscopy (FCS) is a method of investigating concentration fluctuations of fluorescent particles typically in the nM range as a result of its femtoliter-sized sample volume. However, biological processes on cell membranes that involve molecules in the μM concentration ran...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AIP Publishing LLC
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8179723/ https://www.ncbi.nlm.nih.gov/pubmed/34104537 http://dx.doi.org/10.1063/5.0051679 |
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author | Chandler, Joseph M. Xu, Huizhong |
author_facet | Chandler, Joseph M. Xu, Huizhong |
author_sort | Chandler, Joseph M. |
collection | PubMed |
description | Fluorescence Correlation Spectroscopy (FCS) is a method of investigating concentration fluctuations of fluorescent particles typically in the nM range as a result of its femtoliter-sized sample volume. However, biological processes on cell membranes that involve molecules in the μM concentration range require sample volumes well below the conventional FCS limit as well as nanoscale confinement in the longitudinal direction. In this study, we show that an effective measurement volume down to the zeptoliter range can be achieved via the introduction of a nanowire waveguide, resulting in an illumination spot of about 50 nm in lateral dimensions and a longitudinal confinement of around 20 nm just above the waveguide exit surface. Using illumination profiles obtained from finite element method simulations of dielectric nanowaveguides, we perform Monte Carlo simulations of fluorescence fluctuations for two scenarios of fluorophore movement: fluorophores freely diffusing in the three-dimensional (3D) space above the nanowaveguide and fluorophores moving in a two-dimensional (2D) membrane situated directly above the nanowaveguide exit surface. We have developed analytical functions to fit the simulation results and found that an effective illumination size of about 150 zl and 4 × 10(−3) µm(2) can be obtained for the 3D and 2D scenarios, respectively. Given the flat surface geometry and the deep-subwavelength confinement of its illumination spot, this nanowaveguide-illuminated fluorescence correlation spectroscopy technique may be well suited for studying the concentration and dynamics of densely distributed protein molecules on cell membranes. |
format | Online Article Text |
id | pubmed-8179723 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | AIP Publishing LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-81797232021-06-07 Nanowaveguide-illuminated fluorescence correlation spectroscopy for single molecule studies Chandler, Joseph M. Xu, Huizhong AIP Adv Regular Articles Fluorescence Correlation Spectroscopy (FCS) is a method of investigating concentration fluctuations of fluorescent particles typically in the nM range as a result of its femtoliter-sized sample volume. However, biological processes on cell membranes that involve molecules in the μM concentration range require sample volumes well below the conventional FCS limit as well as nanoscale confinement in the longitudinal direction. In this study, we show that an effective measurement volume down to the zeptoliter range can be achieved via the introduction of a nanowire waveguide, resulting in an illumination spot of about 50 nm in lateral dimensions and a longitudinal confinement of around 20 nm just above the waveguide exit surface. Using illumination profiles obtained from finite element method simulations of dielectric nanowaveguides, we perform Monte Carlo simulations of fluorescence fluctuations for two scenarios of fluorophore movement: fluorophores freely diffusing in the three-dimensional (3D) space above the nanowaveguide and fluorophores moving in a two-dimensional (2D) membrane situated directly above the nanowaveguide exit surface. We have developed analytical functions to fit the simulation results and found that an effective illumination size of about 150 zl and 4 × 10(−3) µm(2) can be obtained for the 3D and 2D scenarios, respectively. Given the flat surface geometry and the deep-subwavelength confinement of its illumination spot, this nanowaveguide-illuminated fluorescence correlation spectroscopy technique may be well suited for studying the concentration and dynamics of densely distributed protein molecules on cell membranes. AIP Publishing LLC 2021-06-04 /pmc/articles/PMC8179723/ /pubmed/34104537 http://dx.doi.org/10.1063/5.0051679 Text en © 2021 Author(s). https://creativecommons.org/licenses/by/4.0/All article content, except where otherwise noted, is licensed under a Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ). |
spellingShingle | Regular Articles Chandler, Joseph M. Xu, Huizhong Nanowaveguide-illuminated fluorescence correlation spectroscopy for single molecule studies |
title | Nanowaveguide-illuminated fluorescence correlation spectroscopy for single molecule studies |
title_full | Nanowaveguide-illuminated fluorescence correlation spectroscopy for single molecule studies |
title_fullStr | Nanowaveguide-illuminated fluorescence correlation spectroscopy for single molecule studies |
title_full_unstemmed | Nanowaveguide-illuminated fluorescence correlation spectroscopy for single molecule studies |
title_short | Nanowaveguide-illuminated fluorescence correlation spectroscopy for single molecule studies |
title_sort | nanowaveguide-illuminated fluorescence correlation spectroscopy for single molecule studies |
topic | Regular Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8179723/ https://www.ncbi.nlm.nih.gov/pubmed/34104537 http://dx.doi.org/10.1063/5.0051679 |
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