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. 2022 Jan 12;13:290. doi: 10.1038/s41467-021-27915-z

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© The Author(s) 2022

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 5 — A Cryo-EM map for the gerbil prestin structure (colored by subunit in cyan and yellow, respectively) showing the surrounding micelle as a gray transparent surface. The dashed line (in navy) follows the micelle’s boundaries. The micelle belt around the transmembrane domain of prestin is locally distorted (thinned) at the cytosolic side close to TM6 and TM12 helices. The approximate thickness of the micelle in these regions is indicated by black arrows. The transmembrane helices 6, 7, and 12 are labeled. B As in (A) but tilted by ~10° to better illustrate the micelle’s distortions at the cytosolic side. See also Supplementary Fig. 9.