Download MendeleyCryo-EM structure of the human concentrative nucleoside transporter CNT3.
Zhou, Y.X., Liao, L.H., Wang, C., Li, J.L., Chi, P., Xiao, Q.J., Liu, Q., Guo, L., Sun, L.F., Deng, D.(2020) PLoS Biol 18: e3000790-e3000790
- PubMed: 32776918
- DOI: https://doi.org/10.1371/journal.pbio.3000790
- Primary Citation of Related Structures:
6KSW - PubMed Abstract:
Concentrative nucleoside transporters (CNTs), members of the solute carrier (SLC) 28 transporter family, facilitate the salvage of nucleosides and therapeutic nucleoside derivatives across the plasma membrane. Despite decades of investigation, the structures of human CNTs remain unknown. We determined the cryogenic electron microscopy (cryo-EM) structure of human CNT (hCNT) 3 at an overall resolution of 3.6 Å. As with its bacterial homologs, hCNT3 presents a trimeric architecture with additional N-terminal transmembrane helices to stabilize the conserved central domains. The conserved binding sites for the substrate and sodium ions unravel the selective nucleoside transport and distinct coupling mechanism. Structural comparison of hCNT3 with bacterial homologs indicates that hCNT3 is stabilized in an inward-facing conformation. This study provides the molecular determinants for the transport mechanism of hCNTs and potentially facilitates the design of nucleoside drugs.
Organizational Affiliation:
Division of Obstetrics, Key Laboratory of Birth Defects and Related Disease of Women and Children of MOE, State Key Laboratory of Biotherapy, West China Second Hospital, Sichuan University, Chengdu, China.
