Asymmetric pendrin homodimer reveals its molecular mechanism as anion exchanger

• Published in: Nature communications 2023-05, Vol.14 (1), p.3012-3012, Article 3012
• Main Authors: Liu, Qianying, Zhang, Xiang, Huang, Hui, Chen, Yuxin, Wang, Fang, Hao, Aihua, Zhan, Wuqiang, Mao, Qiyu, Hu, Yuxia, Han, Lin, Sun, Yifang, Zhang, Meng, Liu, Zhimin, Li, Geng-Lin, Zhang, Weijia, Shu, Yilai, Sun, Lei, Chen, Zhenguo
• Format: Article
• Language: English
• Subjects: 101/28; 631/45/612/1237; 631/535/1258/1259; 631/57/2270/1140; 631/57/2283; Ablation; Animals; Anion exchange; Anion exchanging; Anions; Asymmetry; Binding sites; Blood pressure; Cryoelectron Microscopy; Electron microscopy; Genetic disorders; Goiter; Goiter, Nodular - genetics; Hearing loss; Humanities and Social Sciences; Hypothyroidism; Laboratories; Membrane Transport Proteins - genetics; Mice; Microscopy; Molecular modelling; Molecular structure; multidisciplinary; Mutation; Neurosciences; Otolaryngology; Protein Subunits; Science; Science (multidisciplinary); Secretion; Structure-function relationships; Sulfate Transporters - genetics; Thyroid gland
• ISSN: 2041-1723; 2041-1723
• DOI: 10.1038/s41467-023-38303-0

Pendrin (SLC26A4) is an anion exchanger expressed in the apical membranes of selected epithelia. Pendrin ablation causes Pendred syndrome, a genetic disorder associated with sensorineural hearing loss, hypothyroid goiter, and reduced blood pressure. However its molecular structure has remained unknown, limiting our understanding of the structural basis of transport. Here, we determine the cryo-electron microscopy structures of mouse pendrin with symmetric and asymmetric homodimer conformations. The asymmetric homodimer consists of one inward-facing protomer and the other outward-facing protomer, representing coincident uptake and secretion- a unique state of pendrin as an electroneutral exchanger. The multiple conformations presented here provide an inverted alternate-access mechanism for anion exchange. The structural and functional data presented here disclose the properties of an anion exchange cleft and help understand the importance of disease-associated variants, which will shed light on the pendrin exchange mechanism. Pendrin SLC26A4 plays an important role for anion balance. Here, authors resolve cryo-EM structures of pendrin performing co-incident uptake and secretion of anions, providing a structural basis of this anion exchange mechanism.