Significance: Pentameric ligand-gated ion channels (pLGICs) control membrane conductance in living systems from bacteria to humans. Molecular dynamics simulations based on the structures of the prokaryotic channels fromGloeobacter violaceus(GLIC) andErwinia chrysanthemi(ELIC) and the eukaryotic channel fromCaenorhabditis elegans(GluCl) show that the open-to-closed transition begins with a major quaternary (twisting) transition which is followed by tertiary relaxation of the pore-forming helices. The latter is initiated by the outward tilting of the extracellular β-sandwiches in response to agonist unbinding. The proposed atomic resolution mechanism for channel gating, which is in accord with the Monod–Wyman–Changeux model of allostery, is expected to be generally applicable to pLGICs.

Plastids have retained from their cyanobacterial ancestor a fragment of the respiratory electron chain comprising an NADPH dehydrogenase and a diiron oxidase, which sustain the so-called chlororespiration pathway. Despite its very low turnover rates compared with photosynthetic electron flow, knocking out the plastid terminal oxidase (PTOX) in plants or microalgae leads to severe phenotypes that encompass developmental and growth defects together with increased photosensitivity. On the basis of a phylogenetic and structural analysis of the enzyme, we discuss its physiological contribution to chloroplast metabolism, with an emphasis on its critical function in setting the redox poise of the chloroplast stroma in darkness. The emerging picture of PTOX is that of an enzyme at the crossroads of a variety of metabolic processes, such as, among others, the regulation of cyclic electron transfer and carotenoid biosynthesis, which have in common their dependence on the redox state of the plastoquinone pool, set largely by the activity of PTOX in darkness.