reviewAnnual Review of BiochemistryApr 7, 2006Closed access

Protein Misfolding, Functional Amyloid, and Human Disease

University of Florence · University of Cambridge

PubMed
Indexed incrossrefpubmed

Abstract

Peptides or proteins convert under some conditions from their soluble forms into highly ordered fibrillar aggregates. Such transitions can give rise to pathological conditions ranging from neurodegenerative disorders to systemic amyloidoses. In this review, we identify the diseases known to be associated with formation of fibrillar aggregates and the specific peptides and proteins involved in each case. We describe, in addition, that living organisms can take advantage of the inherent ability of proteins to form such structures to generate novel and diverse biological functions. We review recent advances toward the elucidation of the structures of amyloid fibrils and the mechanisms of their formation at a…

Citation impact

6,402
total citations
FWCI
113.18
Percentile
100%
References
194
Citations per year

Authors

2

Topics & keywords

Keywords
  • Amyloid fibril
  • Protein aggregation
  • Amyloid (mycology)
  • Fibril
  • Protein folding
  • Chemistry
  • Amyloid disease
  • Computational biology
UN Sustainable Development Goals
  • Life in Land
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