PT - JOURNAL ARTICLE AU - Lowry, Augustus J. AU - Liang, Pengfei AU - Song, Mo AU - Wan, Y.C. Serena AU - Pei, Zhen-Ming AU - Yang, Huanghe AU - Zhang, Yang TI - TMEM16 and OSCA/TMEM63 proteins share a conserved potential to permeate ions and phospholipids AID - 10.1101/2024.02.04.578431 DP - 2024 Jan 01 TA - bioRxiv PG - 2024.02.04.578431 4099 - http://biorxiv.org/content/early/2024/09/03/2024.02.04.578431.short 4100 - http://biorxiv.org/content/early/2024/09/03/2024.02.04.578431.full AB - The calcium-activated TMEM16 proteins and the mechanosensitive/osmolarity-activated OSCA/TMEM63 proteins belong to the Transmembrane Channel/Scramblase (TCS) superfamily. Within the superfamily, OSCA/TMEM63 proteins, as well as TMEM16A and TMEM16B, are thought to function solely as ion channels. However, most TMEM16 members, including TMEM16F, maintain an additional function as scramblases, rapidly exchanging phospholipids between leaflets of the membrane. Although recent studies have advanced our understanding of TCS structure-function relationships, the molecular determinants of TCS ion and lipid permeation remain unclear. Here we show that single mutations along the transmembrane helix (TM) 4/6 interface allow non-scrambling TCS members to permeate phospholipids. In particular, this study highlights the key role of TM 4 in controlling TCS ion and lipid permeation and offers novel insights into the evolution of the TCS superfamily, suggesting that, like TMEM16s, the OSCA/TMEM63 family maintains a conserved potential to permeate ions and phospholipids.Competing Interest StatementThe authors have declared no competing interest.