Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Más filtros




Base de datos
Intervalo de año de publicación
1.
Sci Rep ; 8(1): 16014, 2018 10 30.
Artículo en Inglés | MEDLINE | ID: mdl-30375424

RESUMEN

Peroxisomal matrix proteins contain either a peroxisomal targeting sequence 1 (PTS1) or a PTS2 that are recognized by the import receptors PEX5 and PEX7, respectively. PEX5 transports the PTS1 proteins and the PEX7/PTS2 complex to the docking translocation module (DTM) at the peroxisomal membrane. After cargo release PEX5 is monoubiquitinated and extracted from the peroxisomal membrane by the receptor export machinery (REM) comprising PEX26 and the AAA ATPases PEX1 and PEX6. Here, we investigated the protein interactions of monoubiquitinated PEX5 with the docking proteins PEX13, PEX14 and the REM. "Click" chemistry was used to synthesise monoubiquitinated recombinant PEX5. We found that monoubiquitinated PEX5 binds the PEX7/PTS2 complex and restores PTS2 protein import in vivo in ΔPEX5 fibroblasts. In vitro pull-down assays revealed an interaction of recombinant PEX5 and monoubiquitinated PEX5 with PEX13, PEX14 and with the REM components PEX1, PEX6 and PEX26. The interactions with the docking proteins were independent of the PEX5 ubiquitination status whereas the interactions with the REM components were increased when PEX5 is ubiquitinated.


Asunto(s)
Receptor de la Señal 1 de Direccionamiento al Peroxisoma/química , Peroxisomas/química , Mapas de Interacción de Proteínas/genética , Transporte de Proteínas/genética , ATPasas Asociadas con Actividades Celulares Diversas/química , ATPasas Asociadas con Actividades Celulares Diversas/genética , Secuencia de Aminoácidos/genética , Animales , Química Clic , Citosol/química , Citosol/metabolismo , Fibroblastos/química , Humanos , Proteínas de la Membrana/química , Proteínas de la Membrana/genética , Ratones , Simulación del Acoplamiento Molecular , Mutación , Receptor de la Señal 2 de Direccionamiento al Peroxisoma/química , Receptor de la Señal 2 de Direccionamiento al Peroxisoma/genética , Señales de Direccionamiento al Peroxisoma/genética , Receptor de la Señal 1 de Direccionamiento al Peroxisoma/genética , Peroxisomas/genética , Ubiquitina/química , Ubiquitina/metabolismo , Ubiquitinación/genética
2.
J Biol Chem ; 293(29): 11553-11563, 2018 07 20.
Artículo en Inglés | MEDLINE | ID: mdl-29884772

RESUMEN

PEX1 and PEX6 are two members of the ATPases associated with diverse cellular activities (AAA) family and the core components of the receptor export module of the peroxisomal matrix protein import machinery. Their role is to extract monoubiquitinated PEX5, the peroxisomal protein-shuttling receptor, from the peroxisomal membrane docking/translocation module (DTM), so that a new cycle of protein transportation can start. Recent data have shown that PEX1 and PEX6 form a heterohexameric complex that unfolds substrates by processive threading. However, whether the natural substrate of the PEX1-PEX6 complex is monoubiquitinated PEX5 (Ub-PEX5) itself or some Ub-PEX5-interacting component(s) of the DTM remains unknown. In this work, we used an established cell-free in vitro system coupled with photoaffinity cross-linking and protein PEGylation assays to address this problem. We provide evidence suggesting that DTM-embedded Ub-PEX5 interacts directly with both PEX1 and PEX6 through its ubiquitin moiety and that the PEX5 polypeptide chain is globally unfolded during the ATP-dependent extraction event. These findings strongly suggest that DTM-embedded Ub-PEX5 is a bona fide substrate of the PEX1-PEX6 complex.


Asunto(s)
ATPasas Asociadas con Actividades Celulares Diversas/metabolismo , Citosol/metabolismo , Proteínas de la Membrana/metabolismo , Receptor de la Señal 1 de Direccionamiento al Peroxisoma/metabolismo , Mapas de Interacción de Proteínas , Humanos , Modelos Moleculares , Receptor de la Señal 1 de Direccionamiento al Peroxisoma/química , Peroxisomas/metabolismo , Transporte de Proteínas , Desplegamiento Proteico , Ubiquitina/metabolismo , Ubiquitinación
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA