» Articles » PMID: 39715905

Wide-ranging Cellular Functions of Ion Channels and Lipid Scramblases in the Structurally Related TMC, TMEM16 and TMEM63 Families

Overview
Date 2024 Dec 23
PMID 39715905
Authors
Affiliations
Soon will be listed here.
Abstract

Calcium (Ca)-activated ion channels and lipid scramblases in the transmembrane protein 16 (TMEM16) family are structurally related to mechanosensitive ion channels in the TMEM63 and transmembrane channel-like (TMC) families. Members of this structurally related superfamily share similarities in gating transitions and serve a wide range of physiological functions, which is evident from their disease associations. The TMEM16, TMEM63 and TMC families include members with important functions in the cell membrane and/or intracellular organelles such as the endoplasmic reticulum, membrane contact sites, endosomes and lysosomes. Moreover, some members of the TMEM16 family and the TMC family perform dual functions of ion channel and lipid scramblase, leading to intriguing physiological implications. In addition to their physiological functions such as mediating phosphatidylserine exposure and facilitation of extracellular vesicle generation and cell fusion, scramblases are involved in the entry and replication of enveloped viruses. Comparisons of structurally diverse scramblases may uncover features in the lipid-scrambling mechanisms that are likely shared by scramblases.

References
1.
Brunner J, Lim N, Schenck S, Duerst A, Dutzler R . X-ray structure of a calcium-activated TMEM16 lipid scramblase. Nature. 2014; 516(7530):207-12. DOI: 10.1038/nature13984. View

2.
Paulino C, Neldner Y, Lam A, Kalienkova V, Brunner J, Schenck S . Structural basis for anion conduction in the calcium-activated chloride channel TMEM16A. Elife. 2017; 6. PMC: 5470873. DOI: 10.7554/eLife.26232. View

3.
Paulino C, Kalienkova V, Lam A, Neldner Y, Dutzler R . Activation mechanism of the calcium-activated chloride channel TMEM16A revealed by cryo-EM. Nature. 2017; 552(7685):421-425. DOI: 10.1038/nature24652. View

4.
Dang S, Feng S, Tien J, Peters C, Bulkley D, Lolicato M . Cryo-EM structures of the TMEM16A calcium-activated chloride channel. Nature. 2017; 552(7685):426-429. PMC: 5750132. DOI: 10.1038/nature25024. View

5.
Lam A, Rutz S, Dutzler R . Inhibition mechanism of the chloride channel TMEM16A by the pore blocker 1PBC. Nat Commun. 2022; 13(1):2798. PMC: 9120017. DOI: 10.1038/s41467-022-30479-1. View