» Articles » PMID: 33658434

Ca Sensitivity of Anoctamin 6/TMEM16F Is Regulated by the Putative Ca-Binding Reservoir at the N-Terminal Domain

Overview
Journal Mol Cells
Publisher Elsevier
Date 2021 Mar 4
PMID 33658434
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Anoctamin 6/TMEM16F (ANO6) is a dual-function protein with Ca-activated ion channel and Ca-activated phospholipid scramblase activities, requiring a high intracellular Ca concentration (e.g., half-maximal effective Ca concentration [EC] of [Ca]i > 10 μM), and strong and sustained depolarization above 0 mV. Structural comparison with Anoctamin 1/TMEM16A (ANO1), a canonical Ca- activated chloride channel exhibiting higher Ca sensitivity (EC of 1 μM) than ANO6, suggested that a homologous Ca-transferring site in the N-terminal domain (Nt) might be responsible for the differential Ca sensitivity and kinetics of activation between ANO6 and ANO1. To elucidate the role of the putative Ca-transferring reservoir in the Nt (Nt-CaRes), we constructed an ANO6-1-6 chimera in which Nt-CaRes was replaced with the corresponding domain of ANO1. ANO6- 1-6 showed higher sensitivity to Ca than ANO6. However, neither the speed of activation nor the voltage-dependence differed between ANO6 and ANO6-1-6. Molecular dynamics simulation revealed a reduced Ca interaction with Nt- CaRes in ANO6 than ANO6-1-6. Moreover, mutations on potentially Ca-interacting acidic amino acids in ANO6 Nt- CaRes resulted in reduced Ca sensitivity, implying direct interactions of Ca with these residues. Based on these results, we cautiously suggest that the net charge of Nt- CaRes is responsible for the difference in Ca sensitivity between ANO1 and ANO6.

Citing Articles

Polymodal Control of TMEM16x Channels and Scramblases.

Agostinelli E, Tammaro P Int J Mol Sci. 2022; 23(3).

PMID: 35163502 PMC: 8835819. DOI: 10.3390/ijms23031580.


Roles, molecular mechanisms, and signaling pathways of TMEMs in neurological diseases.

Chen Q, Fang J, Shen H, Chen L, Shi M, Huang X Am J Transl Res. 2022; 13(12):13273-13297.

PMID: 35035675 PMC: 8748174.


Gating and Regulatory Mechanisms of TMEM16 Ion Channels and Scramblases.

Le S, Liang P, Lowry A, Yang H Front Physiol. 2021; 12:787773.

PMID: 34867487 PMC: 8640346. DOI: 10.3389/fphys.2021.787773.


Intramolecular Disulfide Bonds for Biogenesis of CALHM1 Ion Channel Are Dispensable for Voltage-Dependent Activation.

Kwon J, Jeon Y, Kim J, Kim S, Kim S Mol Cells. 2021; 44(10):758-769.

PMID: 34711692 PMC: 8560582. DOI: 10.14348/molcells.2021.0131.

References
1.
Grubb S, Poulsen K, Juul C, Kyed T, Klausen T, Larsen E . TMEM16F (Anoctamin 6), an anion channel of delayed Ca(2+) activation. J Gen Physiol. 2013; 141(5):585-600. PMC: 3639583. DOI: 10.1085/jgp.201210861. View

2.
Feng S, Dang S, Han T, Ye W, Jin P, Cheng T . Cryo-EM Studies of TMEM16F Calcium-Activated Ion Channel Suggest Features Important for Lipid Scrambling. Cell Rep. 2019; 28(2):567-579.e4. PMC: 6684876. DOI: 10.1016/j.celrep.2019.06.023. View

3.
Xiao Q, Yu K, Perez-Cornejo P, Cui Y, Arreola J, Hartzell H . Voltage- and calcium-dependent gating of TMEM16A/Ano1 chloride channels are physically coupled by the first intracellular loop. Proc Natl Acad Sci U S A. 2011; 108(21):8891-6. PMC: 3102354. DOI: 10.1073/pnas.1102147108. View

4.
Humphrey W, Dalke A, Schulten K . VMD: visual molecular dynamics. J Mol Graph. 1996; 14(1):33-8, 27-8. DOI: 10.1016/0263-7855(96)00018-5. View

5.
Caputo A, Caci E, Ferrera L, Pedemonte N, Barsanti C, Sondo E . TMEM16A, a membrane protein associated with calcium-dependent chloride channel activity. Science. 2008; 322(5901):590-4. DOI: 10.1126/science.1163518. View