IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v7y2016i1d10.1038_ncomms12178.html
   My bibliography  Save this article

Monitoring G protein-coupled receptor and β-arrestin trafficking in live cells using enhanced bystander BRET

Author

Listed:
  • Yoon Namkung

    (Research Institute of the McGill University Health Center (RI-MUHC), McGill University)

  • Christian Le Gouill

    (Université de Montréal)

  • Viktoria Lukashova

    (Université de Montréal)

  • Hiroyuki Kobayashi

    (Université de Montréal)

  • Mireille Hogue

    (Université de Montréal)

  • Etienne Khoury

    (Research Institute of the McGill University Health Center (RI-MUHC), McGill University)

  • Mideum Song

    (Research Institute of the McGill University Health Center (RI-MUHC), McGill University)

  • Michel Bouvier

    (Université de Montréal)

  • Stéphane A. Laporte

    (Research Institute of the McGill University Health Center (RI-MUHC), McGill University
    McGill University
    McGill University)

Abstract

Endocytosis and intracellular trafficking of receptors are pivotal to maintain physiological functions and drug action; however, robust quantitative approaches are lacking to study such processes in live cells. Here we present new bioluminescence resonance energy transfer (BRET) sensors to quantitatively monitor G protein-coupled receptors (GPCRs) and β-arrestin trafficking. These sensors are based on bystander BRET and use the naturally interacting chromophores luciferase (RLuc) and green fluorescent protein (rGFP) from Renilla. The versatility and robustness of this approach are exemplified by anchoring rGFP at the plasma membrane or in endosomes to generate high dynamic spectrometric BRET signals on ligand-promoted recruitment or sequestration of RLuc-tagged proteins to, or from, specific cell compartments, as well as sensitive subcellular BRET imaging for protein translocation visualization. These sensors are scalable to high-throughput formats and allow quantitative pharmacological studies of GPCR trafficking in real time, in live cells, revealing ligand-dependent biased trafficking of receptor/β-arrestin complexes.

Suggested Citation

  • Yoon Namkung & Christian Le Gouill & Viktoria Lukashova & Hiroyuki Kobayashi & Mireille Hogue & Etienne Khoury & Mideum Song & Michel Bouvier & Stéphane A. Laporte, 2016. "Monitoring G protein-coupled receptor and β-arrestin trafficking in live cells using enhanced bystander BRET," Nature Communications, Nature, vol. 7(1), pages 1-12, November.
  • Handle: RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms12178
    DOI: 10.1038/ncomms12178
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/ncomms12178
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/ncomms12178?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms12178. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.