Mobility of Lower MA-Helices for Ion Conduction through Lateral Portals in 5-HT3A Receptors

Abstract

The intracellular domain of the serotonin type 3A receptor, a pentameric ligand-gated ion channel, is crucial for regulating conductance. Ion permeation through the extracellular vestibule and the transmembrane channel is well understood, whereas the specific ion conduction pathway through the intracellular domain is less clear. The intracellular domain starts with a short loop after the third transmembrane segment, followed by a short a-helical segment, a large unstructured loop, and finally, the membrane-associated MA-helix that continues into the last transmembrane segment. The MA-helices from all five subunits form the extension of the transmembrane ion channel and shape what has been described as a ''closed vestibule,'' with their lateral portals obstructed by loops and their cytosolic ends forming a tight hydrophobic constriction. The question remains whether the lateral portals or cytosolic constriction conduct ions upon channel opening. In our study, we used disulfide bond formation between pairs of engineered cysteines to probe the proximity and mobility of segments of the MA-helices most distal to the membrane bilayer. Our results indicate that the proximity and orientation for cysteine pairs at I409C/R410C, in close proximity to the lateral windows, and L402C/L403C, at the cytosolic ends of the MA-helices, are conducive for disulfide bond formation. Although conformational changes associated with gating promote cross-linking for I409C/R410C, which in turn decreases channel currents, cross-linking of L402C/L403C is functionally silent in macroscopic currents. These results support the hypothesis that concerted conformational changes open the lateral portals for ion conduction, rendering ion conduction through the vertical portal unlikely.

The MA Helix Is Important for Receptor Assembly and Function in the α4β2 nACh Receptor

“…Wild-type rat α4β2 nAChRs containing an L9'A mutation in the M2 helix of the α4 subunits (to enhance receptor responses to ligand [24,25], referred to as WT in the following text) showed concentration-dependent fluorescent responses to nicotine addition, revealing a pEC 50 of 7.6 ± 0.12 (EC 50 = 25.3 nM), similar to previous work [18], and a Hill slope (n H ) of 0.8 ± 0.2 (Figure 3). Mutant receptors with similar EC 50 values exhibited similar concentration-response curves (Figure 3D).…”