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Immiscible inclusion bodies formed by polyglutamine and poly(glycine-alanine) are enriched with distinct proteomes but converge in proteins that are risk factors for disease and involved in protein degradation

Poly(glycine-alanine) (polyGA) is one of the polydipeptides expressed in Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 caused by C9ORF72 mutations and accumulates as inclusion bodies in the brain of patients. Superficially these inclusions are similar to those formed by polyglutamin...

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Detalles Bibliográficos
Autores principales: Radwan, Mona, Lilley, Jordan D., Ang, Ching-Seng, Reid, Gavin E., Hatters, Danny M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7455042/
https://www.ncbi.nlm.nih.gov/pubmed/32857759
http://dx.doi.org/10.1371/journal.pone.0233247

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