Quantification of Protein Levels in Single Living Cells

Accurate measurement of the amount of specific protein a cell produces is important for investigating basic molecular processes. We have developed a technique that allows for quantitation of protein levels in single cells in vivo. This protein quantitation ratioing (PQR) technique uses a genetic tag...

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Main Authors: Chiu-An Lo, Ibrahim Kays, Farida Emran, Tsung-Jung Lin, Vedrana Cvetkovska, Brian Edwin Chen
Format: Article
Language:English
Published: Elsevier 2015-12-01
Series:Cell Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124715013637
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spelling doaj-591c93b38ad14c59bb24c3965ce5d9d22020-11-24T21:55:00ZengElsevierCell Reports2211-12472015-12-0113112634264410.1016/j.celrep.2015.11.048Quantification of Protein Levels in Single Living CellsChiu-An Lo0Ibrahim Kays1Farida Emran2Tsung-Jung Lin3Vedrana Cvetkovska4Brian Edwin Chen5Centre for Research in Neuroscience, Research Institute of the McGill University Health Centre, Montréal, QC H3G 1A4, CanadaCentre for Research in Neuroscience, Research Institute of the McGill University Health Centre, Montréal, QC H3G 1A4, CanadaCentre for Research in Neuroscience, Research Institute of the McGill University Health Centre, Montréal, QC H3G 1A4, CanadaCentre for Research in Neuroscience, Research Institute of the McGill University Health Centre, Montréal, QC H3G 1A4, CanadaCentre for Research in Neuroscience, Research Institute of the McGill University Health Centre, Montréal, QC H3G 1A4, CanadaCentre for Research in Neuroscience, Research Institute of the McGill University Health Centre, Montréal, QC H3G 1A4, CanadaAccurate measurement of the amount of specific protein a cell produces is important for investigating basic molecular processes. We have developed a technique that allows for quantitation of protein levels in single cells in vivo. This protein quantitation ratioing (PQR) technique uses a genetic tag that produces a stoichiometric ratio of a fluorescent protein reporter and the protein of interest during protein translation. The fluorescence intensity is proportional to the number of molecules produced of the protein of interest and is used to determine the relative amount of protein within the cell. We use PQR to quantify protein expression of different genes using quantitative imaging, electrophysiology, and phenotype. We use genome editing to insert Protein Quantitation Reporters into endogenous genomic loci in three different genomes for quantitation of endogenous protein levels. The PQR technique will allow for a wide range of quantitative experiments examining gene-to-phenotype relationships with greater accuracy.http://www.sciencedirect.com/science/article/pii/S2211124715013637
collection DOAJ
language English
format Article
sources DOAJ
author Chiu-An Lo
Ibrahim Kays
Farida Emran
Tsung-Jung Lin
Vedrana Cvetkovska
Brian Edwin Chen
spellingShingle Chiu-An Lo
Ibrahim Kays
Farida Emran
Tsung-Jung Lin
Vedrana Cvetkovska
Brian Edwin Chen
Quantification of Protein Levels in Single Living Cells
Cell Reports
author_facet Chiu-An Lo
Ibrahim Kays
Farida Emran
Tsung-Jung Lin
Vedrana Cvetkovska
Brian Edwin Chen
author_sort Chiu-An Lo
title Quantification of Protein Levels in Single Living Cells
title_short Quantification of Protein Levels in Single Living Cells
title_full Quantification of Protein Levels in Single Living Cells
title_fullStr Quantification of Protein Levels in Single Living Cells
title_full_unstemmed Quantification of Protein Levels in Single Living Cells
title_sort quantification of protein levels in single living cells
publisher Elsevier
series Cell Reports
issn 2211-1247
publishDate 2015-12-01
description Accurate measurement of the amount of specific protein a cell produces is important for investigating basic molecular processes. We have developed a technique that allows for quantitation of protein levels in single cells in vivo. This protein quantitation ratioing (PQR) technique uses a genetic tag that produces a stoichiometric ratio of a fluorescent protein reporter and the protein of interest during protein translation. The fluorescence intensity is proportional to the number of molecules produced of the protein of interest and is used to determine the relative amount of protein within the cell. We use PQR to quantify protein expression of different genes using quantitative imaging, electrophysiology, and phenotype. We use genome editing to insert Protein Quantitation Reporters into endogenous genomic loci in three different genomes for quantitation of endogenous protein levels. The PQR technique will allow for a wide range of quantitative experiments examining gene-to-phenotype relationships with greater accuracy.
url http://www.sciencedirect.com/science/article/pii/S2211124715013637
work_keys_str_mv AT chiuanlo quantificationofproteinlevelsinsinglelivingcells
AT ibrahimkays quantificationofproteinlevelsinsinglelivingcells
AT faridaemran quantificationofproteinlevelsinsinglelivingcells
AT tsungjunglin quantificationofproteinlevelsinsinglelivingcells
AT vedranacvetkovska quantificationofproteinlevelsinsinglelivingcells
AT brianedwinchen quantificationofproteinlevelsinsinglelivingcells
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