Cargando…
Amyloid Disassembly: What Can We Learn from Chaperones?
Protein aggregation and subsequent accumulation of insoluble amyloid fibrils with cross-β structure is an intrinsic characteristic of amyloid diseases, i.e., amyloidoses. Amyloid formation involves a series of on-pathway and off-pathway protein aggregation events, leading to mature insoluble fibrils...
Autores principales: | Almeida, Zaida L., Brito, Rui M. M. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9776232/ https://www.ncbi.nlm.nih.gov/pubmed/36552032 http://dx.doi.org/10.3390/biomedicines10123276 |
Ejemplares similares
-
Amyloid assembly and disassembly
por: Chuang, Edward, et al.
Publicado: (2018) -
Mechanistic Insights into the Role of Molecular Chaperones in Protein Misfolding Diseases: From Molecular Recognition to Amyloid Disassembly
por: Hervás, Rubén, et al.
Publicado: (2020) -
Structure and Aggregation Mechanisms in Amyloids
por: L. Almeida, Zaida, et al.
Publicado: (2020) -
Unzipping the Secrets of Amyloid Disassembly by the Human Disaggregase
por: Franco, Aitor, et al.
Publicado: (2021) -
Abundant neuroprotective chaperone Lipocalin-type prostaglandin D synthase (L-PGDS) disassembles the Amyloid-β fibrils
por: Kannaian, Bhuvaneswari, et al.
Publicado: (2019)