Supattapone Surachai
From the Departments of Biochemistry and Medicine, Geisel School of Medicine at Dartmouth, Hanover, New Hampshire 03755
J Biol Chem. 2014 Jul 18;289(29):19850-4. doi: 10.1074/jbc.R113.511329. Epub 2014 May 23.
Recently, synthetic prions with a high level of specific infectivity have been produced from chemically defined components in vitro. A major insight arising from these studies is that various classes of host-encoded cofactor molecules such as phosphatidylethanolamine and RNA molecules are required to form and maintain the specific conformation of infectious prions. Synthetic mouse prions formed with phosphatidylethanolamine exhibit levels of specific infectivity ∼1 million-fold greater than "protein-only" prions (Deleault, N. R., Walsh, D. J., Piro, J. R., Wang, F., Wang, X., Ma, J., Rees, J. R., and Supattapone, S. (2012) Proc. Natl. Acad. Sci. U.S.A. 109, E1938-E1946). Moreover, cofactor molecules also appear to regulate prion strain properties by limiting the potential conformations of the prion protein (see Deleault et al. above). The production of fully infectious synthetic prions provides new opportunities to study the mechanism of prion infectivity directly by structural and biochemical methods.
最近,已在体外由化学成分明确的组分产生了具有高特异性感染性的合成朊病毒。这些研究得出的一个主要见解是,需要各类宿主编码的辅助因子分子,如磷脂酰乙醇胺和RNA分子,来形成并维持感染性朊病毒的特定构象。由磷脂酰乙醇胺形成的合成小鼠朊病毒的特异性感染水平比“仅蛋白质”朊病毒高约100万倍(Deleault,N.R.,Walsh,D.J.,Piro,J.R.,Wang,F.,Wang,X.,Ma,J.,Rees,J.R.,和Supattapone,S.(2012年)《美国国家科学院院刊》109,E1938 - E1946)。此外,辅助因子分子似乎还通过限制朊病毒蛋白的潜在构象来调节朊病毒株的特性(见上文Deleault等人的研究)。完全感染性合成朊病毒的产生为通过结构和生化方法直接研究朊病毒感染机制提供了新机会。