A novel hotspot of gelsolin instability triggers an alternative mechanism of amyloid aggregation

Gelsolin comprises six homologous domains, named G1 to G6. Single point substitutions in this protein are responsible for AGel amyloidosis, a hereditary disease causing progressive corneal lattice dystrophy, cutis laxa, and polyneuropathy. Although several different amyloidogenic variants of gelsoli...

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Detalles Bibliográficos
Autores principales: Bollati, Michela, Diomede, Luisa, Giorgino, Toni, Natale, Carmina, Fagnani, Elisa, Boniardi, Irene, Barbiroli, Alberto, Alemani, Rebecca, Beeg, Marten, Gobbi, Marco, Fakin, Ana, Mastrangelo, Eloise, Milani, Mario, Presciuttini, Gianluca, Gabellieri, Edi, Cioni, Patrizia, de Rosa, Matteo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research Network of Computational and Structural Biotechnology 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8649582/
https://www.ncbi.nlm.nih.gov/pubmed/34938411
http://dx.doi.org/10.1016/j.csbj.2021.11.025

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8649582/
https://www.ncbi.nlm.nih.gov/pubmed/34938411
http://dx.doi.org/10.1016/j.csbj.2021.11.025

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