Literature DB >> 28389201

Optical measurement of receptor tyrosine kinase oligomerization on live cells.

Inhee Chung1.   

Abstract

Receptor tyrosine kinases (RTK) are important cell surface receptors that transduce extracellular signals across the plasma membrane. The traditional view of how these receptors function is that ligand binding to the extracellular domains acts as a master-switch that enables receptor monomers to dimerize and subsequently trans-phosphorylate each other on their intracellular domains. However, a growing body of evidence suggests that receptor oligomerization is not merely a consequence of ligand binding, but is instead part of a complex process responsible for regulation of receptor activation. Importantly, the oligomerization dynamics and subsequent activation of these receptors are affected by other cellular components, such as cytoskeletal machineries and cell membrane lipid characteristics. Thus receptor activation is not an isolated molecular event mediated by the ligand-receptor interaction, but instead involves orchestrated interactions between the receptors and other cellular components. Measuring receptor oligomerization dynamics on live cells can yield important insights into the characteristics of these interactions. Therefore, it is imperative to develop techniques that can probe receptor movements on the plasma membrane with optimal temporal and spatial resolutions. Various microscopic techniques have been used for this purpose. Optical techniques including single molecule tracking (SMT) and fluorescence correlation spectroscopy (FCS) measure receptor diffusion on live cells. Receptor-receptor interactions can also be assessed by detecting Förster resonance energy transfer (FRET) between fluorescently-labeled receptors situated in close proximity or by counting the number of receptors within a diffraction limited fluorescence spot (stepwise bleaching). This review will describe recent developments of optical techniques that have been used to study receptor oligomerization on living cells. This article is part of a Special Issue entitled: Interactions between membrane receptors in cellular membranes edited by Kalina Hristova.
Copyright © 2017 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Activation mechanism; Oligomerization; Optical measurement on live cells; Receptor tyrosine kinase (RTK)

Mesh:

Substances:

Year:  2017        PMID: 28389201     DOI: 10.1016/j.bbamem.2017.03.026

Source DB:  PubMed          Journal:  Biochim Biophys Acta Biomembr        ISSN: 0005-2736            Impact factor:   3.747


  4 in total

1.  Multiscale Simulations of Biological Membranes: The Challenge To Understand Biological Phenomena in a Living Substance.

Authors:  Giray Enkavi; Matti Javanainen; Waldemar Kulig; Tomasz Róg; Ilpo Vattulainen
Journal:  Chem Rev       Date:  2019-03-12       Impact factor: 60.622

2.  Endoplasmic reticulum stress activates human IRE1α through reversible assembly of inactive dimers into small oligomers.

Authors:  Vladislav Belyy; Iratxe Zuazo-Gaztelu; Andrew Alamban; Avi Ashkenazi; Peter Walter
Journal:  Elife       Date:  2022-06-22       Impact factor: 8.713

3.  Conjugation of Fab' Fragments with Fluorescent Dyes for Single-Molecule Tracking On Live Cells.

Authors:  I-Ting Teng; Xiangning Bu; Inhee Chung
Journal:  Bio Protoc       Date:  2019-09-20

Review 4.  Single-molecule fluorescence vistas of how lipids regulate membrane proteins.

Authors:  Alyssa E Ward; Yujie Ye; Jennifer A Schuster; Shushu Wei; Francisco N Barrera
Journal:  Biochem Soc Trans       Date:  2021-08-27       Impact factor: 5.407

  4 in total

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