Literature DB >> 35451749

Absolute Quantification of Plasma Membrane Receptors Via Quantitative Flow Cytometry.

Yingye Fang1,2, Manasi Malik3, Sarah K England3, P I Imoukhuede4.   

Abstract

Plasma membrane receptors are transmembrane proteins that initiate cellular response following the binding of specific ligands (e.g., growth factors, hormones, and cytokines). The abundance of plasma membrane receptors can be a diagnostic or prognostic biomarker in many human diseases. One of the best techniques for measuring plasma membrane receptors is quantitative flow cytometry (qFlow). qFlow employs fluorophore-conjugated antibodies against the receptors of interest and corresponding fluorophore-loaded calibration beads offers standardized and reproducible measurements of plasma membrane receptors. More importantly, qFlow can achieve absolute quantification of plasma membrane receptors when phycoerythrin (PE) is the fluorophore of choice. Here we describe a detailed qFlow protocol to obtain absolute receptor quantities on the basis of PE calibration. This protocol is foundational for many previous and ongoing studies in quantifying tyrosine kinase receptors and G-protein-coupled receptors with in vitro cell models and ex vivo cell samples.
© 2022. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Biomarker; Phycoerythrin (PE); Protein quantification; Quantitative flow cytometry; RTK

Mesh:

Substances:

Year:  2022        PMID: 35451749      PMCID: PMC9261967          DOI: 10.1007/978-1-0716-2217-9_4

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  28 in total

1.  Two-step protocol for preparing adherent cells for high-throughput flow cytometry.

Authors:  Mandeep Kaur; Luke Esau
Journal:  Biotechniques       Date:  2015-09-01       Impact factor: 1.993

2.  Flow cytometry controls, instrument setup, and the determination of positivity.

Authors:  Holden T Maecker; Joseph Trotter
Journal:  Cytometry A       Date:  2006-09-01       Impact factor: 4.355

3.  Compensation in flow cytometry.

Authors:  Mario Roederer
Journal:  Curr Protoc Cytom       Date:  2002-12

4.  qFlow Cytometry-Based Receptoromic Screening: A High-Throughput Quantification Approach Informing Biomarker Selection and Nanosensor Development.

Authors:  Si Chen; Jared Weddell; Pavan Gupta; Grace Conard; James Parkin; Princess I Imoukhuede
Journal:  Methods Mol Biol       Date:  2017

5.  Effects of Different Cell-Detaching Methods on the Viability and Cell Surface Antigen Expression of Synovial Mesenchymal Stem Cells.

Authors:  Kunikazu Tsuji; Miyoko Ojima; Koji Otabe; Masafumi Horie; Hideyuki Koga; Ichiro Sekiya; Takeshi Muneta
Journal:  Cell Transplant       Date:  2017-01-31       Impact factor: 4.064

6.  A Quantitative Method for Comparing the Brightness of Antibody-dye Reagents and Estimating Antibodies Bound per Cell.

Authors:  Aaron B Kantor; Wayne A Moore; Stephen Meehan; David R Parks
Journal:  Curr Protoc Cytom       Date:  2016-07-01

7.  Performance evaluation of QuantiBRITE phycoerythrin beads.

Authors:  K K Pannu; E T Joe; S B Iyer
Journal:  Cytometry       Date:  2001-12-01

Review 8.  Cell signaling by receptor tyrosine kinases.

Authors:  Mark A Lemmon; Joseph Schlessinger
Journal:  Cell       Date:  2010-06-25       Impact factor: 41.582

9.  Optimized flow cytometry protocol for analysis of surface expression of interleukin-1 receptor types I and II.

Authors:  Filipp Filippovich Vasilyev; Julia Anatolievna Lopatnikova; Sergey Vitalievich Sennikov
Journal:  Cytotechnology       Date:  2013-02-26       Impact factor: 2.058

10.  Endothelial CD276 (B7-H3) expression is increased in human malignancies and distinguishes between normal and tumour-derived circulating endothelial cells.

Authors:  J Kraan; P van den Broek; C Verhoef; D J Grunhagen; W Taal; J W Gratama; S Sleijfer
Journal:  Br J Cancer       Date:  2014-06-03       Impact factor: 7.640

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