Next Article in Journal
Coagulatory Defects in Type-1 and Type-2 Diabetes
Next Article in Special Issue
TLQP-21, A VGF-Derived Peptide Endowed of Endocrine and Extraendocrine Properties: Focus on In Vitro Calcium Signaling
Previous Article in Journal
Cancer Cell-Derived Granulocyte-Macrophage Colony-Stimulating Factor Is Dispensable for the Progression of 4T1 Murine Breast Cancer
Previous Article in Special Issue
Calcium Signaling in ß-cell Physiology and Pathology: A Revisit
Open AccessReview

Partners in Crime: Towards New Ways of Targeting Calcium Channels

1
Univ. Lille, Inserm, U1003-PHYCEL-Physiologie Cellulaire, F-59000 Lille, France
2
Laboratory of Excellence, Ion Channels Science and Therapeutics, Université de Lille, 59655 Villeneuve d’Ascq, France
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2019, 20(24), 6344; https://doi.org/10.3390/ijms20246344
Received: 5 November 2019 / Revised: 5 December 2019 / Accepted: 13 December 2019 / Published: 16 December 2019
(This article belongs to the Special Issue Calcium Signaling in Human Health and Diseases 2.0)
The characterization of calcium channel interactome in the last decades opened a new way of perceiving ion channel function and regulation. Partner proteins of ion channels can now be considered as major components of the calcium homeostatic mechanisms, while the reinforcement or disruption of their interaction with the channel units now represents an attractive target in research and therapeutics. In this review we will focus on the targeting of calcium channel partner proteins in order to act on the channel activity, and on its consequences for cell and organism physiology. Given the recent advances in the partner proteins’ identification, characterization, as well as in the resolution of their interaction domain structures, we will develop the latest findings on the interacting proteins of the following channels: voltage-dependent calcium channels, transient receptor potential and ORAI channels, and inositol 1,4,5-trisphosphate receptor. View Full-Text
Keywords: TRP channel; CaV channel; domain interactions; TCAF; Rap; IP3R; sigma receptor TRP channel; CaV channel; domain interactions; TCAF; Rap; IP3R; sigma receptor
Show Figures

Figure 1

MDPI and ACS Style

Noyer, L.; Lemonnier, L.; Mariot, P.; Gkika, D. Partners in Crime: Towards New Ways of Targeting Calcium Channels. Int. J. Mol. Sci. 2019, 20, 6344.

Show more citation formats Show less citations formats
Note that from the first issue of 2016, MDPI journals use article numbers instead of page numbers. See further details here.

Article Access Map by Country/Region

1
Back to TopTop