Department of Chemistry, Department of Physiology and Functional Genomics, Center for Research at Bio/Nano Interface, UF Health Cancer Center , UF Genetics Institute and McKnight Brain Institute, University of Florida , Gainesville , Florida 32611-7200 , United States.
Department of Emergency Medicine, Department of Chemistry, Department of Neuroscience, and Department of Psychiatry , McKnight Brain Institute, University of Florida , Gainesville , Florida 32611 , United States.
J Am Chem Soc. 2018 Oct 31;140(43):14314-14323. doi: 10.1021/jacs.8b08645. Epub 2018 Oct 16.
Tau proteins are proteins that stabilize microtubules, but their hyperphosphorylation can result in the formation of protein aggregates and, over time, neurodegeneration. This phenomenon, termed tauopathy, is pathologically involved in several neurodegenerative disorders. DNA aptamers are single-stranded oligonucleotides capable of specific binding to target molecules. Using tau epitopes predisposed for phosphorylation, we identified six distinct aptamers that bind to tau at two phosphorylatable epitopes (Thr-231 and Ser-202) and to full-length Tau441 proteins with nanomolar affinity. In addition, several of these aptamers also inhibit tau phosphorylation (IT4, IT5, IT6) and tau oligomerization (IT3, IT4, IT5, IT6). This is the first report to identify tau epitope-specific aptamers. Such tau aptamers can be used to detect tau in biofluids and uncover the mechanism of tauopathy. They can be further developed into novel therapeutic agents in mitigating tauopathy-associated neurodegenerative disorders.
tau 蛋白是稳定微管的蛋白质,但它们的过度磷酸化会导致蛋白质聚集的形成,随着时间的推移,还会导致神经退行性变。这种现象被称为 tau 病,与几种神经退行性疾病的病理有关。DNA 适体是能够与靶分子特异性结合的单链寡核苷酸。使用易发生磷酸化的 tau 表位,我们鉴定出六个不同的适体,它们与 tau 在两个可磷酸化表位(Thr-231 和 Ser-202)结合,并与全长 Tau441 蛋白以纳摩尔亲和力结合。此外,这些适体中的几个还可以抑制 tau 磷酸化(IT4、IT5、IT6)和 tau 寡聚化(IT3、IT4、IT5、IT6)。这是首次报道鉴定 tau 表位特异性适体。这种 tau 适体可用于检测生物流体中的 tau,并揭示 tau 病的机制。它们可以进一步开发成减轻与 tau 病相关的神经退行性疾病的新型治疗剂。