Carregant...
Miniatura

Tipus de document

Article

Versió

Versió publicada

Data de publicació

Llicència de publicació

cc-by (c) Sabaté Lagunas, Raimon et al., 2015
Si us plau utilitzeu sempre aquest identificador per citar o enllaçar aquest document: https://hdl.handle.net/2445/102347

What Makes a Protein Sequence a Prion?

Títol de la revista

Director/Tutor

ISSN de la revista

Títol del volum

Resum

Typical amyloid diseases such as Alzheimer's and Parkinson's were thought to exclusively result from de novo aggregation, but recently it was shown that amyloids formed in one cell can cross-seed aggregation in other cells, following a prion-like mechanism. Despite the large experimental effort devoted to understanding the phenomenon of prion transmissibility, it is still poorly understood how this property is encoded in the primary sequence. In many cases, prion structural conversion is driven by the presence of relatively large glutamine/asparagine (Q/N) enriched segments. Several studies suggest that it is the amino acid composition of these regions rather than their specific sequence that accounts for their priogenicity. However, our analysis indicates that it is instead the presence and potency of specific short amyloid-prone sequences that occur within intrinsically disordered Q/N-rich regions that determine their prion behaviour, modulated by the structural and compositional context. This provides a basis for the accurate identification and evaluation of prion candidate sequences in proteomes in the context of a unified framework for amyloid formation and prion propagation.

Citació

Citació

SABATÉ LAGUNAS, Raimon, ROUSSEAU, Frederic, SCHYMKOWITZ, Joost, VENTURA, Salvador. What Makes a Protein Sequence a Prion?. _PLoS Computational Biology_. 2015. Vol. 11, núm. 1, pàgs. e1004013. [consulta: 25 de febrer de 2026]. ISSN: 1553-734X. [Disponible a: https://hdl.handle.net/2445/102347]

Exportar metadades

JSON - METS

Compartir registre