From the Department of Experimental and Clinical Biomedical Sciences "Mario Serio," University of Florence, Viale G. B. Morgagni 50, 50134, Firenze, Italy.
the Dipartimento di Scienze Biochimiche "A. Rossi Fanelli," Sapienza University of Rome, 00185 Rome, Italy, and.
J Biol Chem. 2018 Jun 29;293(26):10303-10313. doi: 10.1074/jbc.RA118.002087. Epub 2018 May 14.
A set of missense mutations in the gene encoding profilin-1 has been linked to the onset of familial forms of ALS (fALS), also known as Lou Gehrig's disease. The pathogenic potential of these mutations is linked to the formation of intracellular inclusions of the mutant proteins and correlates with the mutation-induced destabilization of its native, fully folded state. However, the mechanism by which these mutations promote misfolding and self-assembly is yet unclear. Here, using temperature-jump and stopped-flow kinetic measurements, we show that, during refolding, WT profilin-1 transiently populates a partially folded (PF) state endowed with hydrophobic clusters exposed to the solvent and with no detectable secondary structure. We observed that this conformational state is marginally stable at neutral pH but becomes significantly populated at mildly acidic pH. Interestingly, the fALS-associated mutations did not cause a change in the refolding mechanism of profilin-1, but induced a stabilization of the PF state. In the presence of preformed profilin-1 aggregates, the PF state, unlike the unfolded and folded states, could interact with these aggregates via nonspecific hydrophobic interactions and also increase thioflavin-T fluorescence, revealing its amyloidogenic potential. Moreover, in the variants tested, we found a correlation between conformational stability of PF and aggregation propensity, defining this conformational state as an aggregation-prone folding intermediate. In conclusion, our findings indicate that mutation-induced stabilization of a partially folded state can enhance profilin-1 aggregation and thereby contribute to the pathogenicity of the mutations.
一组编码原肌球蛋白-1 的错义突变与家族性肌萎缩侧索硬化症(fALS)的发病有关,也称为葛雷克氏症。这些突变的致病性与突变蛋白的细胞内包含体的形成有关,并且与突变诱导的其天然完全折叠状态的不稳定性相关。然而,这些突变促进错误折叠和自组装的机制尚不清楚。在这里,我们使用温度跳跃和停流动力学测量,表明在重折叠过程中,WT 原肌球蛋白-1短暂地占据了具有暴露于溶剂的疏水性簇的部分折叠(PF)状态,并且没有检测到二级结构。我们观察到这种构象状态在中性 pH 下略微稳定,但在轻度酸性 pH 下明显增加。有趣的是,fALS 相关突变没有改变原肌球蛋白-1的重折叠机制,但诱导了 PF 状态的稳定。在预形成的原肌球蛋白-1聚集体的存在下,PF 状态与未折叠和折叠状态不同,它可以通过非特异性疏水相互作用与这些聚集体相互作用,并且还可以增加硫黄素-T 荧光,显示其淀粉样形成潜力。此外,在测试的变体中,我们发现 PF 的构象稳定性与聚集倾向之间存在相关性,将该构象状态定义为易于聚集的折叠中间体。总之,我们的发现表明,突变诱导的部分折叠状态的稳定性增加可以增强原肌球蛋白-1的聚集,从而有助于突变的致病性。