Physical basis of apparent pore-dilation of ATP-activated P2X receptor channels The selectivity of ion channels is fundamental for their roles in electrical and chemical signaling, and ion homeostasis. Although most ion channels exhibit stable ion selectivity, the prevailing view for purinergic P2X receptor channels, transient receptor potential V1 (TRPV1) channels and acid sensing ion channels (ASICs) is that their ion conduction pores dilate upon prolonged activation. We investigated this mechanism in P2X receptors and found that the hallmark shift in equilibrium potential observed with prolonged channel activation does not result from pore dilation, but from time-dependent alterations in the concentration of intracellular ions. We derived a physical model to calculate ion concentration changes during whole-cell patch-clamp recordings, which validates our experimental findings and provides a quantitative guideline for effectively controlling ion concentration. We have also developed a physical model for both the inside-out and out-side out configurations of patch-clamp recordings, which reveal much faster kinetics for ion depletion and accumulation compared to whole-cell recording. Our results have fundamental implications for understanding ion permeation and gating in P2X receptor channels, and more broadly for using patch-clamp techniques to study ion channels and neuronal excitability.

Project Start
Project End
Budget Start
Budget End
Support Year
12
Fiscal Year
2018
Total Cost
Indirect Cost
City
State
Country
Zip Code
Li, Mufeng; Toombes, Gilman E S; Silberberg, Shai D et al. (2015) Physical basis of apparent pore dilation of ATP-activated P2X receptor channels. Nat Neurosci 18:1577-83
Heymann, Gabriel; Dai, Jian; Li, Mufeng et al. (2013) Inter- and intrasubunit interactions between transmembrane helices in the open state of P2X receptor channels. Proc Natl Acad Sci U S A 110:E4045-54
Li, Mufeng; Silberberg, Shai D; Swartz, Kenton J (2013) Subtype-specific control of P2X receptor channel signaling by ATP and Mg2+. Proc Natl Acad Sci U S A 110:E3455-63
Kawate, Toshimitsu; Robertson, Janice L; Li, Mufeng et al. (2011) Ion access pathway to the transmembrane pore in P2X receptor channels. J Gen Physiol 137:579-90
Silberberg, Shai D; Swartz, Kenton J (2009) Structural biology: Trimeric ion-channel design. Nature 460:580-1
Li, Mufeng; Chang, Tsg-Hui; Silberberg, Shai D et al. (2008) Gating the pore of P2X receptor channels. Nat Neurosci 11:883-7
Silberberg, Shai D; Li, Mufeng; Swartz, Kenton J (2007) Ivermectin Interaction with transmembrane helices reveals widespread rearrangements during opening of P2X receptor channels. Neuron 54:263-74