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 c... More
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.
