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Recovery of functional enzyme from amyloid fibrils.
Agócs, Gergely; Solymosi, Katalin; Varga, Andrea; Módos, Károly; Kellermayer, Miklós; Závodszky, Péter; Fidy, Judit; Osváth, Szabolcs.
  • Agócs G; Department of Biophysics and Radiation Biology, Semmelweis University, Budapest, Hungary.
FEBS Lett ; 584(6): 1139-42, 2010 Mar 19.
Article en En | MEDLINE | ID: mdl-20132817
ABSTRACT
Amyloid deposits, which accumulate in numerous diseases, are the final stage of multi-step protein conformational-conversion and oligomerization processes. The underlying molecular mechanisms are not fully understood, and particularly little is known about the reverse reaction. Here we show that phosphoglycerate kinase amyloid fibrils can be converted back into native protein. We achieved recovery with 60% efficiency, which is comparable to the success rate of the unfolding-refolding studies, and the recovered enzyme was folded, stable and fully active. The key intermediate stages in the recovery process are fibril disassembly and unfolding followed by spontaneous protein folding.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Fosfoglicerato Quinasa / Amiloide Tipo de estudio: Diagnostic_studies Idioma: En Año: 2010 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Fosfoglicerato Quinasa / Amiloide Tipo de estudio: Diagnostic_studies Idioma: En Año: 2010 Tipo del documento: Article