Observation of Structural Changes on Activation of the NTS1 G-Protein-Coupled Receptor on DNA-Templated Protein Arrays by cryo-EM

Abstract

and transmembrane domains M1-M3, and the other the fourth transmembrane domain M4) results in the assembly of functional pLGICs indistinguishable in their electrophysiological properties from wt pLGICs assembled from contiguous subunits. Alanine scanning of M1, M3 and M4 of the GlyR a1 subunit identified a total of 12 aromatic residues as important or crucial for pentameric assembly. The assembly-relevant aromatic residues cluster in one face of each helix. Homology modelling based on crystal structures (Hilf & Dutzler 2008; Bocquet et al 2008) predicted p-p interactions between the aromatic face of the M4 helix and three or two aromatic residues located in the M1 helix (Tyr228, Trp239, and Phe242) and the M3 helix (Trp286, Phe293), respectively . The loss of homopentamer formation and function seen upon alanine replacement of any of these contact residues strongly supports the existence of a membrane-embedded network of pairwisely interacting aromatic side chains that compacts and stabilizes the membrane core region of the GlyR. We infer from these results that a precise geometric arrangement of transmembrane helices defined by the tri-helical aromatic network is a prerequisite to allow the circular arrangement of the subunits stabilized essentially by earlier occurring random subunit interactions between the ectodomains.