Plasticity of the selectivity filter is essential for permeation in lysosomal TPC2 channels

• 成果类型: Article
• 署名作者: Zaki, Afroditi-Mario; Cinaroglu, Sueleyman Selim; Rahman, Taufiq; Patel, Sandip; Biggin, Philip C.
• 署名单位: University of Oxford; University of Cambridge; University of London; University College London; Ege University
• 刊物名称: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
• ISSN/ISSBN: 0027-9301
• DOI: 10.1073/pnas.2320153121
• 发表日期: 2024-08-06
• 关键词: particle mesh ewald; ion permeation; molecular-dynamics; voltage; ca2+; mechanism; simulations; organelles; calcium

摘要

Two- pore channels are pathophysiologically important Na+- and Ca2+- permeable channels expressed in lysosomes and other acidic organelles. Unlike most other ion channels, their permeability is malleable and ligand- tuned such that when gated by the signaling lipid PI(3,5)P2, they are more Na+- selective than when gated by the Ca2+ mobilizing messenger nicotinic acid adenine dinucleotide phosphate. However, the structural basis that underlies such plasticity and single- channel behavior more generally remains poorly understood. A recent Cryo- electron microscopy (cryo- EM) structure of TPC2 bound to PI(3,5)P2 in a proposed open- channel conformation provided an opportunity to address this via molecular dynamics (MD) simulation. To our surprise, simulations designed to compute conductance through this structure revealed almost no Na+ permeation events even at very high transmembrane voltages. However further MD simulations identified a spontaneous transition to a dramatically different conformation of the selectivity filter that involved expansion and a flip in the orientation of two core asparagine residues. This alternative filter conformation was remarkably stable and allowed Na+ to flow through the channel leading to a conductance estimate that was in very good agreement with direct single- channel measurements. Furthermore, this conformation was more permeable for Na+ over Ca2+. Our results have important ramifications not just for understanding the control of ion selectivity in TPC2 channels but also more broadly in terms of how ion channels discriminate ions.