SwePub
Sök i LIBRIS databas

  Extended search

WFRF:(Brorsson C.)
 

Search: WFRF:(Brorsson C.) > (2010-2014) > Intrinsic determina...

  • Brorsson, Ann-ChristinUniversity of Cambridge (author)

Intrinsic determinants of neurotoxic aggregate formation by the amyloid beta peptide

  • Article/chapterEnglish2010

Publisher, publication year, extent ...

  • Elsevier BV,2010
  • printrdacarrier

Numbers

  • LIBRIS-ID:oai:DiVA.org:liu-60811
  • https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-60811URI
  • https://doi.org/10.1016/j.bpj.2009.12.4320DOI

Supplementary language notes

  • Language:English
  • Summary in:English

Part of subdatabase

Classification

  • Subject category:ref swepub-contenttype
  • Subject category:art swepub-publicationtype

Notes

  • The extent to which proteins aggregate into distinct structures ranging from prefibrillar oligomers to amyloid fibrils is key to the pathogenesis of many age-related degenerative diseases. We describe here for the Alzheimer's disease-related amyloid beta peptide (Abeta) an investigation of the sequence-based determinants of the balance between the formation of prefibrillar aggregates and amyloid fibrils. We show that by introducing single-point mutations, it is possible to convert the normally harmless Abeta40 peptide into a pathogenic species by increasing its relative propensity to form prefibrillar but not fibrillar aggregates, and, conversely, to abolish the pathogenicity of the highly neurotoxic E22G Abeta42 peptide by reducing its relative propensity to form prefibrillar species rather than mature fibrillar ones. This observation can be rationalized by the demonstration that whereas regions of the sequence of high aggregation propensity dominate the overall tendency to aggregate, regions with low intrinsic aggregation propensities exert significant control over the balance of the prefibrillar and fibrillar species formed, and therefore play a major role in determining the neurotoxicity of the Abeta peptide.

Subject headings and genre

  • MEDICINE
  • MEDICIN

Added entries (persons, corporate bodies, meetings, titles ...)

  • Bolognesi, BenedettaUniversity of Cambridge (author)
  • Tartaglia, Gian GaetanoUniversity of Cambridge (author)
  • Shammas, Sarah LUniversity of Cambridge (author)
  • Favrin, GiorgioUniversity of Cambridge (author)
  • Watson, IanUniversity of Cambridge (author)
  • Lomas, David AUniversity of Cambridge (author)
  • Chiti, FabrizioUniversità degli Studi di Firenze, Italy (author)
  • Vendruscolo, MicheleUniversity of Cambridge (author)
  • Dobson, Christopher MUniversity of Cambridge (author)
  • Crowther, Damian CUniversity of Cambridge (author)
  • Luheshi, Leila MUniversity of Cambridge (author)
  • University of CambridgeUniversità degli Studi di Firenze, Italy (creator_code:org_t)

Related titles

  • In:Biophysical Journal: Elsevier BV98:8, s. 1677-840006-34951542-0086

Internet link

Find in a library

To the university's database

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Close

Copy and save the link in order to return to this view