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Total Internal Reflection Fluorescence Quantification of Receptor Pharmacology

Total internal reflection fluorescence (TIRF) microscopy has been widely used as a single molecule imaging technique to study various fundamental aspects of cell biology, owing to its ability to selectively excite a very thin fluorescent volume immediately above the substrate on which the cells are...

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Autor principal: Fang, Ye
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4493547/
https://www.ncbi.nlm.nih.gov/pubmed/25922915
http://dx.doi.org/10.3390/bios5020223
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author Fang, Ye
author_facet Fang, Ye
author_sort Fang, Ye
collection PubMed
description Total internal reflection fluorescence (TIRF) microscopy has been widely used as a single molecule imaging technique to study various fundamental aspects of cell biology, owing to its ability to selectively excite a very thin fluorescent volume immediately above the substrate on which the cells are grown. However, TIRF microscopy has found little use in high content screening due to its complexity in instrumental setup and experimental procedures. Inspired by the recent demonstration of label-free evanescent wave biosensors for cell phenotypic profiling and drug screening with high throughput, we had hypothesized and demonstrated that TIRF imaging is also amenable to receptor pharmacology profiling. This paper reviews key considerations and recent applications of TIRF imaging for pharmacology profiling.
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spelling pubmed-44935472015-07-07 Total Internal Reflection Fluorescence Quantification of Receptor Pharmacology Fang, Ye Biosensors (Basel) Review Total internal reflection fluorescence (TIRF) microscopy has been widely used as a single molecule imaging technique to study various fundamental aspects of cell biology, owing to its ability to selectively excite a very thin fluorescent volume immediately above the substrate on which the cells are grown. However, TIRF microscopy has found little use in high content screening due to its complexity in instrumental setup and experimental procedures. Inspired by the recent demonstration of label-free evanescent wave biosensors for cell phenotypic profiling and drug screening with high throughput, we had hypothesized and demonstrated that TIRF imaging is also amenable to receptor pharmacology profiling. This paper reviews key considerations and recent applications of TIRF imaging for pharmacology profiling. MDPI 2015-04-27 /pmc/articles/PMC4493547/ /pubmed/25922915 http://dx.doi.org/10.3390/bios5020223 Text en © 2015 by the author; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Fang, Ye
Total Internal Reflection Fluorescence Quantification of Receptor Pharmacology
title Total Internal Reflection Fluorescence Quantification of Receptor Pharmacology
title_full Total Internal Reflection Fluorescence Quantification of Receptor Pharmacology
title_fullStr Total Internal Reflection Fluorescence Quantification of Receptor Pharmacology
title_full_unstemmed Total Internal Reflection Fluorescence Quantification of Receptor Pharmacology
title_short Total Internal Reflection Fluorescence Quantification of Receptor Pharmacology
title_sort total internal reflection fluorescence quantification of receptor pharmacology
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4493547/
https://www.ncbi.nlm.nih.gov/pubmed/25922915
http://dx.doi.org/10.3390/bios5020223
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