Stabilizing effects of geraniol on native and pathogenic M39R rhodopsin variants

Introduction: Mutations in rhodopsin are a major cause of autosomal dominant retinitis pigmentosa, frequently due to protein misfolding and reduced structural stability. The M391.34R variant, located in transmembrane helix 1, is associated with sector retinitis pigmentosa and exhibits pronounced the...

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Detalles Bibliográficos
Autores: Fernández González, Pol|||0000-0001-6136-763X, Das, Jenifar, Cruz Sáez, Alejandro|||0000-0003-0928-0718, Pérez González, Juan Jesús|||0000-0002-0748-8147, Garriga Solé, Pere|||0000-0003-4234-8382
Tipo de recurso: artículo
Fecha de publicación:2026
País:España
Institución:Universitat Politècnica de Catalunya (UPC)
Repositorio:UPCommons. Portal del coneixement obert de la UPC
Idioma:inglés
OAI Identifier:oai:upcommons.upc.edu:2117/459535
Acceso en línea:https://hdl.handle.net/2117/459535
https://dx.doi.org/10.3389/fnins.2026.1799935
Access Level:acceso abierto
Palabra clave:Protein misfolding
Retinal degeneration
Retinitis pigmentosa
Rhodopsin
Visual phototransduction
Àrees temàtiques de la UPC::Enginyeria química
Descripción
Sumario:Introduction: Mutations in rhodopsin are a major cause of autosomal dominant retinitis pigmentosa, frequently due to protein misfolding and reduced structural stability. The M391.34R variant, located in transmembrane helix 1, is associated with sector retinitis pigmentosa and exhibits pronounced thermal and chemical destabilization.Methods: We investigated whether geraniol, a natural monoterpenoid alcohol with reported cytoprotective properties, can act as a pharmacological stabilizer of rhodopsin. Using purified pigments from bovine rod outer segments and recombinant wild-type and M391.34R variants, we assessed photochemical integrity, thermal denaturation, hydroxylamine susceptibility, regeneration kinetics and Meta II fluorescence responses in the presence or absence of geraniol.Results: Geraniol did not interfere with chromophore binding, photobleaching, regeneration, or acid-induced Schiff base protonation. However, it significantly enhanced the thermal and chemical stability of rod outer segments-derived and recombinant wild-type rhodopsin. The M391.34R mutant displayed severe thermal instability and increased susceptibility to hydroxylamine, but geraniol treatment nearly doubled its thermal half-life and improved chromophore retention, although without restoring wild-type stability levels. Remarkably, geraniol induced rapid and marked quenching of Trp2656.48 fluorescence in Meta II, indicating state-dependent interaction with the activated receptor.Discussion: These findings identify geraniol as a membrane-interacting small molecule capable of partially stabilizing structurally compromised rhodopsin variants. While incomplete, the rescue achieved supports the potential of monoterpenoid-based pharmacological chaperones for selected rhodopsin-linked retinal degenerations