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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doaj-fd06251657a045d49fb3df12c11b0fe62020-11-24T23:26:27ZengMDPI AGBiosensors2079-63742015-04-015222324010.3390/bios5020223bios5020223Total Internal Reflection Fluorescence Quantification of Receptor PharmacologyYe Fang0Biochemical Technologies, Science and Technology Division, Corning Incorporated, Corning, NY 14831, USATotal 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.http://www.mdpi.com/2079-6374/5/2/223evanescent wavereceptor pharmacologyresonant waveguide gratingsingle molecule analysissurface plasmon resonancetotal internal reflection fluorescence |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ye Fang |
spellingShingle |
Ye Fang Total Internal Reflection Fluorescence Quantification of Receptor Pharmacology Biosensors evanescent wave receptor pharmacology resonant waveguide grating single molecule analysis surface plasmon resonance total internal reflection fluorescence |
author_facet |
Ye Fang |
author_sort |
Ye Fang |
title |
Total Internal Reflection Fluorescence Quantification of Receptor Pharmacology |
title_short |
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_sort |
total internal reflection fluorescence quantification of receptor pharmacology |
publisher |
MDPI AG |
series |
Biosensors |
issn |
2079-6374 |
publishDate |
2015-04-01 |
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. |
topic |
evanescent wave receptor pharmacology resonant waveguide grating single molecule analysis surface plasmon resonance total internal reflection fluorescence |
url |
http://www.mdpi.com/2079-6374/5/2/223 |
work_keys_str_mv |
AT yefang totalinternalreflectionfluorescencequantificationofreceptorpharmacology |
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1725555056339582976 |