Image mean square displacement to study the lateral mobility of Angiotensin II type 1 and Endothelin 1 type A receptors on living cells

Nadir Planes, Patrick P M L Vanderheyden, Enrico Gratton, Catherina Caballero-George

Research output: Contribution to journalArticlepeer-review

3 Citations (Scopus)

Abstract

The lateral mobility of membrane receptors provides insights into the molecular interactions of protein binding and the complex dynamic plasma membrane. The image mean square displacement (iMSD) analysis is a method used to extract qualitative and quantitative information of the protein diffusion law and infers how diffusion dynamic processes may change when the cellular environment is modified. The aim of the study was to describe the membrane diffusing properties of two G-protein-coupled receptors namely Angiotensin II type 1 (AT1 ) and Endothelin 1 type A (ETA ) receptors and their corresponding receptor-ligand complexes in living cells using total internal reflection fluorescent microscopy and iMSD analysis. This study showed that both AT1 and ETA receptors displayed a mix of three modes of diffusion: free, confined, and partially confined. The confined mode was the predominant at the plasma membrane of living cells and was not affected by ligand binding. However, the local diffusivity and the confinement zone of AT1 receptors were reduced by the binding of its antagonist losartan, and the long-range diffusion with the local diffusivity coefficient of ETA receptors was reduced upon exposure to its antagonist BQ123. To the best of our knowledge, this is the first study addressing the protein diffusion laws of these two receptors on living cells using total internal reflection fluorescence microscopy and iMSD.

Original languageEnglish
Pages (from-to)381-392
Number of pages12
JournalMicroscopy Research and Technique
Volume83
Issue number4
DOIs
Publication statusPublished - Apr 2020

Bibliographical note

Funding Information:
The authors gratefully acknowledge the National Secretariat for Science, Technology and Innovation (SENACYT) of the Republic of Panama for financial support to Dr Caballero‐George and to Ms. Planes through the incentive program of the National Investigation System (SNI) as well as through grant COL10‐070. Thanks are also due to IFARHU from the Panamanian government, which jointly with SENACYT gave a scholarship to Ms. Planes. The authors wish to thank Hongtao Chen for the assistance on the TIRF microscope setup. Dr Gratton acknowledges support from Grants NIH P41‐GM103540 and NIH P50‐GM076516.

Funding Information:
The authors gratefully acknowledge the National Secretariat for Science, Technology and Innovation (SENACYT) of the Republic of Panama for financial support to Dr Caballero-George and to Ms. Planes through the incentive program of the National Investigation System (SNI) as well as through grant COL10-070. Thanks are also due to IFARHU from the Panamanian government, which jointly with SENACYT gave a scholarship to Ms. Planes. The authors wish to thank Hongtao Chen for the assistance on the TIRF microscope setup. Dr Gratton acknowledges support from Grants NIH P41-GM103540 and NIH P50-GM076516.

Publisher Copyright:
© 2019 Wiley Periodicals, Inc.

Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.

Keywords

  • Animals
  • Biological Transport
  • CHO Cells
  • Cricetulus
  • Diffusion
  • Image Processing, Computer-Assisted/methods
  • Microscopy, Fluorescence
  • Protein Binding
  • Receptor, Angiotensin, Type 1/metabolism
  • Receptor, Endothelin A/metabolism

Fingerprint

Dive into the research topics of 'Image mean square displacement to study the lateral mobility of Angiotensin II type 1 and Endothelin 1 type A receptors on living cells'. Together they form a unique fingerprint.

Cite this