Impact of anionic lipids on the energy landscape of conformational transition in anion exchanger 1 (AE1)

Nat Commun. 2025 Nov 26;16(1):11664. doi: 10.1038/s41467-025-66786-6.

Abstract

Anion Exchanger 1 (AE1) is an elevator-type transporter that plays a key role in acid-base homeostasis of erythrocytes. Here, we report three high-resolution cryo-electron microscopy (cryo-EM) structures of distinct states of AE1: two inward-facing (IF1 and IF2) and one outward-facing (OF). Uptake assay revealed the modulatory effect of phosphatidylinositol 4,5-bisphosphate (PIP2) lipids on AE1. Molecular dynamics simulations are conducted on these structures to determine the anion binding sites in AE1. We then use advanced enhanced sampling to study the OF⇌IF transition in AE1 in three systems: apo, HCO3--bound, and an AE1 system in which cryo-EM-determined PIP2 lipids had been removed. The transition pathways were then used to calculate the free energy of the OF⇌IF transition in AE1 under different conditions. The results show how substrate reduces the transition barrier against transport. Furthermore, they capture the inhibitory effect of PIP2 lipids and provide a molecular mechanism for this inhibitory effect.

MeSH terms

  • Anion Exchange Protein 1, Erythrocyte* / chemistry
  • Anion Exchange Protein 1, Erythrocyte* / genetics
  • Anion Exchange Protein 1, Erythrocyte* / metabolism
  • Anion Exchange Protein 1, Erythrocyte* / ultrastructure
  • Anions / chemistry
  • Anions / metabolism
  • Bicarbonates / metabolism
  • Binding Sites
  • Cryoelectron Microscopy
  • Humans
  • Lipids* / chemistry
  • Molecular Dynamics Simulation
  • Phosphatidylinositol 4,5-Diphosphate* / chemistry
  • Phosphatidylinositol 4,5-Diphosphate* / metabolism
  • Protein Conformation

Substances

  • Phosphatidylinositol 4,5-Diphosphate
  • Anion Exchange Protein 1, Erythrocyte
  • Anions
  • Bicarbonates
  • SLC4A1 protein, human
  • Lipids