MRC Prion Unit at UCL, Institute of Prion Diseases, Courtauld Building, 33, Cleveland Street, London W1W 7FF, UK.
Biomolecules. 2022 Nov 16;12(11):1694. doi: 10.3390/biom12111694.
Prion diseases are a class of neurodegenerative diseases that are uniquely infectious. Whilst their general replication mechanism is well understood, the components required for the formation and propagation of highly infectious prions are poorly characterized. The protein-only hypothesis posits that the prion protein (PrP) is the only component of the prion; however, additional co-factors are required for its assembly into infectious prions. These can be provided by brain homogenate, but synthetic lipids and non-coding RNA have also been used in vitro. Here, we review a range of experimental approaches, which generate PrP amyloid assemblies de novo. These synthetic PrP assemblies share some, but not necessarily all, properties of genuine infectious prions. We will discuss the different experimental approaches, how a prion is defined, the non-protein requirements of a prion, and provide an overview of the current state of prion amplification and generation in vitro.
朊病毒病是一类具有独特传染性的神经退行性疾病。尽管其一般复制机制已被充分理解,但对于形成和传播高传染性朊病毒所需的成分仍知之甚少。蛋白质构象假说认为朊病毒蛋白 (PrP) 是朊病毒的唯一成分;然而,其组装成感染性朊病毒还需要其他辅助因子。这些可以由脑匀浆提供,但也可以在体外使用合成脂质和非编码 RNA。在这里,我们回顾了一系列新生成 PrP 淀粉样组装体的实验方法。这些合成的 PrP 组装体具有一些(但不一定是全部)真正感染性朊病毒的特性。我们将讨论不同的实验方法、朊病毒的定义、朊病毒的非蛋白需求,并概述体外朊病毒的扩增和生成的现状。