Determinants shaping the nanoscale architecture of the mouse rod outer segment

dc.contributor.authorPöge, Matthias
dc.contributor.authorMahamid, Julia
dc.contributor.authorImanishi, Sanae S.
dc.contributor.authorPlitzko, Jürgen M.
dc.contributor.authorPalczewski, Krzysztof
dc.contributor.authorBaumeister, Wolfgang
dc.contributor.departmentOphthalmology, School of Medicine
dc.date.accessioned2024-07-02T10:19:01Z
dc.date.available2024-07-02T10:19:01Z
dc.date.issued2021-12-21
dc.description.abstractThe unique membrane organization of the rod outer segment (ROS), the specialized sensory cilium of rod photoreceptor cells, provides the foundation for phototransduction, the initial step in vision. ROS architecture is characterized by a stack of identically shaped and tightly packed membrane disks loaded with the visual receptor rhodopsin. A wide range of genetic aberrations have been reported to compromise ROS ultrastructure, impairing photoreceptor viability and function. Yet, the structural basis giving rise to the remarkably precise arrangement of ROS membrane stacks and the molecular mechanisms underlying genetically inherited diseases remain elusive. Here, cryo-electron tomography (cryo-ET) performed on native ROS at molecular resolution provides insights into key structural determinants of ROS membrane architecture. Our data confirm the existence of two previously observed molecular connectors/spacers which likely contribute to the nanometer-scale precise stacking of the ROS disks. We further provide evidence that the extreme radius of curvature at the disk rims is enforced by a continuous supramolecular assembly composed of peripherin-2 (PRPH2) and rod outer segment membrane protein 1 (ROM1) oligomers. We suggest that together these molecular assemblies constitute the structural basis of the highly specialized ROS functional architecture. Our Cryo-ET data provide novel quantitative and structural information on the molecular architecture in ROS and substantiate previous results on proposed mechanisms underlying pathologies of certain PRPH2 mutations leading to blindness.
dc.eprint.versionFinal published version
dc.identifier.citationPöge M, Mahamid J, Imanishi SS, Plitzko JM, Palczewski K, Baumeister W. Determinants shaping the nanoscale architecture of the mouse rod outer segment. Elife. 2021;10:e72817. Published 2021 Dec 21. doi:10.7554/eLife.72817
dc.identifier.urihttps://hdl.handle.net/1805/42005
dc.language.isoen_US
dc.publishereLife Sciences
dc.relation.isversionof10.7554/eLife.72817
dc.relation.journaleLife
dc.rightsAttribution 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourcePMC
dc.subjectCell biology
dc.subjectDisk rim
dc.subjectMembrane curvature
dc.subjectMolecular biophysics
dc.subjectMouse
dc.subjectPhotoreceptor
dc.subjectProtein scaffold
dc.subjectRod outer segment
dc.subjectStructural biology
dc.titleDeterminants shaping the nanoscale architecture of the mouse rod outer segment
dc.typeArticle
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