Vaccine and Infectious Disease Organization; University of Saskatchewan; Saskatoon, SK Canada; Department of Biochemistry; University of Saskatchewan; Saskatoon, SK Canada.
Prion. 2013 Jul-Aug;7(4):301-11. doi: 10.4161/pri.25148. Epub 2013 May 31.
Transmissible spongiform encephalopathies (TSEs) are fatal neurodegenerative diseases that are based on the misfolding of a cellular prion protein (PrP(C)) into an infectious, pathological conformation (PrP(Sc)). There is proof-of-principle evidence that a prion vaccine is possible but this is tempered with concerns of the potential dangers associated with induction of immune responses to a widely-expressed self-protein. By targeting epitopes that are specifically exposed upon protein misfolding, our group developed a vaccine that induces PrP(Sc)-specific antibody responses. Here we consider the ability of this polyclonal antibody (SN6b) to bind to a mutant of PrP(C) associated with spontaneous prion disease. Polyclonal antibodies were selected to mimic the vaccination outcome and also explore all possible protein conformations of the recombinant bovine prion protein with mutation T194A [bPrP(T194A)]. This mutant is a homolog of the human T183A mutation of PrP(C) that is associated with early onset of familial dementia. With nanopore analysis, under non-denaturing conditions, we observed binding of the SN6b antibody to bPrP(T194A). This interaction was confirmed through ELISAs as well as immunoprecipitation of the recombinant and cellularly expressed forms of bPrP(T194A). This interaction did not promote formation of a protease resistant conformation of PrP in vitro. Collectively, these findings support the disease-specific approach for immunotherapy of prion diseases but also suggest that the concept of conformation-specific immunotherapy may be complicated in individuals who are genetically predisposed to PrP(C) misfolding.
传染性海绵状脑病(TSE)是致命的神经退行性疾病,其基础是细胞朊蛋白(PrP(C))错误折叠成具有感染性和病理性的构象(PrP(Sc))。有原理验证证据表明,朊病毒疫苗是可行的,但这也存在与诱导对广泛表达的自身蛋白的免疫反应相关的潜在危险的担忧。通过针对在蛋白质错误折叠时特异性暴露的表位,我们小组开发了一种能够诱导 PrP(Sc)特异性抗体反应的疫苗。在这里,我们考虑了这种多克隆抗体(SN6b)结合与自发性朊病毒病相关的突变 PrP(C)的能力。选择多克隆抗体来模拟接种结果,并探索重组牛朊病毒蛋白突变 T194A[bPrP(T194A)]的所有可能蛋白质构象。这种突变是与 PrP(C)的人类 T183A 突变同源的,与家族性痴呆症的早期发病有关。通过纳米孔分析,在非变性条件下,我们观察到 SN6b 抗体与 bPrP(T194A)的结合。通过 ELISA 以及对重组和细胞表达形式的 bPrP(T194A)的免疫沉淀,证实了这种相互作用。这种相互作用并没有促进体外 PrP 形成抗蛋白酶抗性构象。总之,这些发现支持针对朊病毒病的免疫疗法的疾病特异性方法,但也表明在遗传易患 PrP(C)错误折叠的个体中,构象特异性免疫疗法的概念可能会变得复杂。