Antibodies towards tyrosine amyloid-like fibrils allow toxicity modulation and cellular imaging of the assemblies

Dor Zaguri, Topaz Kreiser, Shira Shaham-Niv, Ehud Gazit

Research output: Contribution to journalArticlepeer-review

Abstract

The amino acid tyrosine forms cytotoxic amyloid-like fibrils by molecular self-assembly. However, the production of antibodies towards tyrosine assemblies, reflecting their presentation to the immune system, was not demonstrated yet. Here, we describe the production of antibodies that specifically recognize tyrosine in its fibrillated form. The antibodies were demonstrated to specifically bind self-assembled tyrosine, in contrast to its non-aggregated form or disintegrated fibrils. The antibodies could be used for immunostaining of tyrosine fibrils in cultured cells. Furthermore, confocal microscopy allowed a demonstration of the intracellular presence of the metabolite amyloids in a neuroblastoma cell model. Finally, pre-incubation of tyrosine fibrils with the antibodies resulted in significant reduction in their cytotoxicity. Taken together, we provide an experimental proof for the immunogenicity of tyrosine amyloid fibrillary assemblies. These specific antibodies against tyrosine structures could be further used as a research tool to study the dynamics, toxicity and cellular localization of the assemblies.

Original languageEnglish
Article number1273
JournalMolecules
Volume23
Issue number6
DOIs
StatePublished - 2018

Keywords

  • Anti-tyr antibodies
  • Immunogenicity
  • Inborn error of metabolism
  • Metabolite amyloid-like fibrils
  • Self-assembly
  • Tyrosine
  • Tyrosinemia

All Science Journal Classification (ASJC) codes

  • Drug Discovery
  • Analytical Chemistry
  • Chemistry (miscellaneous)
  • Molecular Medicine
  • Physical and Theoretical Chemistry
  • Pharmaceutical Science
  • Organic Chemistry

Fingerprint

Dive into the research topics of 'Antibodies towards tyrosine amyloid-like fibrils allow toxicity modulation and cellular imaging of the assemblies'. Together they form a unique fingerprint.

Cite this