Cited by 336Ion channel regulation and functionIon Transport and Channel RegulationAdvanced Electron Microscopy Techniques and Applications

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Cryo-EM structures of the TMEM16A calcium-activated chloride channel

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Dang, Shangyu, Feng, Shengjie, Tien, Jason, Peters, Christian J., Bulkley, David, Lolicato, Marco, Zhao, Jianhua, Zuberbühler, Kathrin, Ye, Wenlei, Qi, Lijun, Chen, Tingxu, Craik, Charles S., Jan, Yuh Nung, Minor, Daniel L., Cheng, Yifan, Jan, Lily Yeh·2017·Nature

DOI 10.1038/nature25024PMC PMC5750132

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Abstract

Calcium-activated chloride channels (CaCCs) encoded by TMEM16A control neuronal signalling, smooth muscle contraction, airway and exocrine gland secretion, and rhythmic movements of the gastrointestinal system. To understand how CaCCs mediate and control anion permeation to fulfil these physiological functions, knowledge of the mammalian TMEM16A structure and identification of its pore-lining residues are essential. TMEM16A forms a dimer with two pores. Previous CaCC structural analyses have relied on homology modelling of a homologue (nhTMEM16) from the fungus Nectria haematococca that functions primarily as a lipid scramblase, as well as subnanometre-resolution electron cryo-microscopy. Here we present de novo atomic structures of the transmembrane domains of mouse TMEM16A in nanodiscs and in lauryl maltose neopentyl glycol as determined by single-particle electron cryo-microscopy. These structures reveal the ion permeation pore and represent different functional states. The structure in lauryl maltose neopentyl glycol has one Ca 2+ ion resolved within each monomer with a constricted pore; this is likely to correspond to a closed state, because a CaCC with a single Ca 2+ occupancy requires membrane depolarization in order to open (C.J.P. et al., manuscript submitted). The structure in nanodiscs has two Ca 2+ ions per monomer and its pore is in a closed conformation; this probably reflects channel rundown, which is the gradual loss of channel activity that follows prolonged CaCC activation in 1 mM Ca 2+. Our mutagenesis and electrophysiological studies, prompted by analyses of the structures, identified ten residues distributed along the pore that interact with permeant anions and affect anion selectivity, as well as seven pore-lining residues that cluster near pore constrictions and regulate channel gating. Together, these results clarify the basis of CaCC anion conduction.

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Authors: Dang, S., Feng, S., Tien, J., Peters, C. J., Bulkley, D., Lolicato, M., Zhao, J., Zuberbühler, K., Ye, W., Qi, L., Chen, T., Craik, C. S., Jan, Y. N., Minor, D. L., Cheng, Y., & Jan, L. Y.
Affiliations: University of California, San Francisco (US)
Howard Hughes Medical Institute (US)
Lawrence Berkeley National Laboratory (US)
Corresponding author: Cheng, Yifan
Jan, Lily Yeh
ORCID: Dang, Shangyu
Feng, Shengjie
Tien, Jason
Peters, Christian J.
Bulkley, David
Lolicato, Marco
Zhao, Jianhua
Ye, Wenlei
Qi, Lijun
Chen, Tingxu
Craik, Charles S.
Jan, Yuh Nung
Minor, Daniel L.
Cheng, Yifan
Jan, Lily Yeh
Venue: Nature
Publisher: Springer Science and Business Media LLC
Published: 2017-12
Volume: 552
Issue: 7685
Pages: 426-429
ISSN: 0028-0836 (ISSN-L)
1476-4687
DOI: 10.1038/nature25024
PMC: PMC5750132
OpenAlex: W2774013165
Cited by: 333
References: 54
Citations by year: 2026: 16 · 2025: 29 · 2024: 32 · 2023: 28 · 2022: 38 · 2021: 54 · 2020: 40 · 2019: 64 · 2018: 29
FWCI: 15.18
Type: journal article
Language: en
Open access: green
www.ncbi.nlm.nih.gov
Licence: www.springer.com/tdm (tdm)
Locations: Nature (publishedVersion)
PubMed (publishedVersion)
Europe PMC (PubMed Central) (acceptedVersion)
PubMed Central (acceptedVersion)
Rare & Special e-Zone (The Hong Kong University of Science and Technology) (submittedVersion)
RePEc: Research Papers in Economics (submittedVersion)
eScholarship (California Digital Library) (submittedVersion)
Funders: Howard Hughes Medical Institute
National Institutes of Health (1s10od020054-01)
National Heart, Lung, and Blood Institute (R01HL080050)
National Institute on Drug Abuse (K99DA041500)
National Cancer Institute (P41CA196276)
National Institute on Deafness and Other Communication Disorders (R01DC007664)
National Institute of General Medical Sciences (P50GM082250, P01GM111126, R01GM098672)
National Institute of Neurological Disorders and Stroke (R01NS069229, R35NS097227)
Topics: Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion channel regulation and function
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion Transport and Channel Regulation
Life Sciences › Biochemistry, Genetics and Molecular Biology › Structural Biology › Advanced Electron Microscopy Techniques and Applications
Keywords: TMEM16A, calcium-activated chloride channels, TMEM16, channel gating, calcium binding, channel rundown, nanodiscs, detergent solubilization, pore-lining residues, lipid scramblase, channel structure-function relationship
MeSH terms: Anoctamin-1, Animals, Anions, Calcium, Glucosides, Humans, Models, Molecular, Protein Conformation, Ion Channel Gating, Ion Transport, Cryoelectron Microscopy, Nanostructures, Mice, HEK293 Cells

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Cryo-EM structures of the TMEM16A calcium-activated chloride channel

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