Metabolite amyloids: a new paradigm for inborn error of metabolism disorders

Research output: Contribution to journalArticlepeer-review

Abstract

The formation of ordered amyloid assemblies is associated with major human degenerative disorders, including Alzheimer’s disease, Parkinson’s disease, and type 2 diabetes. Amyloid fibrils are elongated nanoscale structures that bind to specific dyes (including thioflavin T and Congo red). Amyloid fibrillar assemblies or their early intermediates are known to induce apoptotic cytotoxic effect. Until recently, amyloid fiber formation was observed only with proteins and peptides. We reported in 2012 that a single amino acid, phenylalanine, could also form typical amyloid fibrils with the same morphology, dye-binding specificity, and electron diffraction pattern as protein amyloids. X-ray crystallography demonstrated the formation of supramolecular β-sheet-like organization by phenylalanine at its zwitterionic form. Metabolite amyloids had pronounced cytotoxicity that could be depleted by treatment with antibodies raised against the phenylalanine structures. We suggested that the observed amyloid formation could explain some of the symptoms observed in phenylketonuria (PKU) upon the accumulation of phenylalanine. Follow-up studies by other groups revealed the ability of phenylalanine amyloids to bind to membranes, as observed with protein amyloids. Furthermore, the doxycycline amyloid formation inhibitor was shown to also affect the formation of phenylalanine amyloids. In 2015, it was reported that other metabolites involved in metabolic disorders, including adenine, uracil, tyrosine, and orotic acid, could form amyloid-like assemblies. It was further demonstrated that the assemblies induce apoptotic cell death. Taken together, we suggest a new hypothesis to understand the etiology of degenerative processes observed in inborn error of metabolism disorders and indicate new avenues for treatment.

Original languageEnglish
Pages (from-to)483-488
Number of pages6
JournalJournal of Inherited Metabolic Disease
Volume39
Issue number4
DOIs
StatePublished - 1 Jul 2016

Fingerprint

Dive into the research topics of 'Metabolite amyloids: a new paradigm for inborn error of metabolism disorders'. Together they form a unique fingerprint.

Cite this