Sabaté Raimon, Baxa Ulrich, Benkemoun Laura, Sánchez de Groot Natalia, Coulary-Salin Bénédicte, Maddelein Marie-Lise, Malato Laurent, Ventura Salvador, Steven Alasdair C, Saupe Sven J
Laboratoire de Génétique Moléculaire des Champignons, Institut de Biochimie et de Génétique Cellulaires,UMR 5095 CNRS/Université de Bordeaux 2, 1 rue Camille St Saëns, 33077 Bordeaux cedex, France.
J Mol Biol. 2007 Jul 20;370(4):768-83. doi: 10.1016/j.jmb.2007.05.014. Epub 2007 May 22.
HET-s is a prion protein of the fungus Podospora anserina. A plausible structural model for the infectious amyloid fold of the HET-s prion-forming domain, HET-s(218-289), makes it an attractive system to study structure-function relationships in amyloid assembly and prion propagation. Here, we report on the diversity of HET-s(218-289) amyloids formed in vitro. We distinguish two types formed at pH 7 from fibrils formed at pH 2, on morphological grounds. Unlike pH 7 fibrils, the pH 2 fibrils show very little if any prion infectivity. They also differ in ThT-binding, resistance to denaturants, assembly kinetics, secondary structure, and intrinsic fluorescence. Both contain 5 nm fibrils, either bundled or disordered (pH 7) or as tightly twisted protofibrils (pH 2). We show that electrostatic interactions are critical for the formation and stability of the infectious prion fold given in the current model. The altered properties of the amyloid assembled at pH 2 may arise from a perturbation in the subunit fold or fibrillar stacking.
HET-s是嗜热栖热放线菌的一种朊病毒蛋白。HET-s朊病毒形成结构域HET-s(218 - 289)的感染性淀粉样折叠的一个合理结构模型,使其成为研究淀粉样蛋白组装和朊病毒传播中结构-功能关系的一个有吸引力的系统。在此,我们报道了体外形成的HET-s(218 - 289)淀粉样蛋白的多样性。基于形态学原因,我们区分了在pH 7条件下形成的两种类型与在pH 2条件下形成的原纤维。与pH 7的原纤维不同,pH 2的原纤维几乎没有朊病毒感染性。它们在硫黄素T结合、对变性剂的抗性、组装动力学、二级结构和固有荧光方面也存在差异。两者都含有5纳米的原纤维,要么成束或无序排列(pH 7),要么是紧密扭曲的原纤维(pH 2)。我们表明,静电相互作用对于当前模型中给出的感染性朊病毒折叠的形成和稳定性至关重要。在pH 2条件下组装的淀粉样蛋白性质的改变可能源于亚基折叠或纤维堆积的扰动。