Metabolite assemblies: A surprising extension to the amyloid hypothesis

Nidhi Gour, Ehud Gazit

Research output: Contribution to journalReview articlepeer-review

Abstract

The realization of the ability of metabolites to form self-assembled amyloid-like nanostructures was a surprising phenomenon. This discovery paved the way towards understanding the pathophysiology of the inborn error of metabolism disorders from a new perspective, relating them to amyloid-associated diseases that are characterized by the aggregation of proteins and polypeptides. Hence, a ‘generic amyloid hypothesis’ can be proposed. This theory implies that the formation of amyloid-like structures is a general phenomenon not limited to proteins and reflects a common etiology for both age-related amyloid-associated diseases and inborn error of metabolism disorders. Here, we present a comprehensive survey of the recent research related to metabolite amyloids including their structure formation through self-association, propagation, interactions, transmission, and their role in metabolic disorders and neurodegenerative diseases and their applications for the fabrication of novel materials which implicate metabolite assemblies as a surprising extension to the amyloid scheme.

Original languageEnglish
Pages (from-to)154-164
Number of pages11
JournalCurrent Opinion in Chemical Biology
Volume64
DOIs
StatePublished - Oct 2021

Keywords

  • Accumulation
  • Amyloid
  • Enzyme dysfunction
  • Gene mutation
  • Inborn errors of metabolism
  • Non-proteinaceous metabolites
  • Self-assembly
  • Single amino acid metabolites
  • Toxicity

All Science Journal Classification (ASJC) codes

  • Analytical Chemistry
  • Biochemistry

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