Author
Listed:
- Amiran Keshelava
(Faculty of Biology and Medicine, University of Lausanne)
- Gonzalo P. Solis
(Faculty of Biology and Medicine, University of Lausanne)
- Micha Hersch
(Faculty of Biology and Medicine, University of Lausanne
Swiss Institute of Bioinformatics)
- Alexey Koval
(Faculty of Biology and Medicine, University of Lausanne)
- Mikhail Kryuchkov
(Faculty of Biology and Medicine, University of Lausanne)
- Sven Bergmann
(Faculty of Biology and Medicine, University of Lausanne
Swiss Institute of Bioinformatics
University of Cape Town)
- Vladimir L. Katanaev
(Faculty of Biology and Medicine, University of Lausanne
School of Biomedicine, Far Eastern Federal University)
Abstract
G protein-coupled receptors (GPCRs) constitute a large family of receptors that activate intracellular signaling pathways upon detecting specific extracellular ligands. While many aspects of GPCR signaling have been uncovered through decades of studies, some fundamental properties, like its channel capacity—a measure of how much information a given transmission system can reliably transduce—are still debated. Previous studies concluded that GPCRs in individual cells could transmit around one bit of information about the concentration of the ligands, allowing only for a reliable on or off response. Using muscarinic receptor-induced calcium response measured in individual cells upon repeated stimulation, we show that GPCR signaling systems possess a significantly higher capacity. We estimate the channel capacity of this system to be above two, implying that at least four concentration levels of the agonist can be distinguished reliably. These findings shed light on the basic principles of GPCR signaling.
Suggested Citation
Amiran Keshelava & Gonzalo P. Solis & Micha Hersch & Alexey Koval & Mikhail Kryuchkov & Sven Bergmann & Vladimir L. Katanaev, 2018.
"High capacity in G protein-coupled receptor signaling,"
Nature Communications, Nature, vol. 9(1), pages 1-8, December.
Handle:
RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-02868-y
DOI: 10.1038/s41467-018-02868-y
Download full text from publisher
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:9:y:2018:i:1:d:10.1038_s41467-018-02868-y. 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.