Department of Biomedical Sciences and Technologies, University of Udine, Piazzale Kolbe 4, 33100 Udine, Italy.
J Biol Chem. 2010 May 7;285(19):14689-700. doi: 10.1074/jbc.M109.082156. Epub 2010 Mar 11.
It has previously been shown that the acylphosphatase from Sulfolobus solfataricus is capable of forming amyloid-like aggregates under conditions in which the native structure is maintained and via the transient formation of native-like aggregates. Based on the previously determined NMR structure of the native protein, showing a ferredoxin-like fold and the peculiar presence of an unstructured N-terminal segment, we show here, at a molecular level using NMR spectroscopy, that indeed S. solfataricus acylphosphatase remains in a native-like conformation when placed in aggregating conditions and that such a native-like structure persists when the protein forms the initial aggregates, at least within the low molecular weight species. The analysis carried out under different solution conditions, based on the measurement of the combined (1)H and (15)N chemical shifts and hydrogen/deuterium exchange rates, enabled the most significant conformational changes to be monitored upon transfer of the monomeric state into aggregating conditions and upon formation of the initial native-like aggregates. Important increases of the hydrogen/deuterium exchange rates throughout the native protein, accompanied by small and localized structural changes, in the monomeric protein were observed. The results also allow the identification of the intermolecular interaction regions within the native-like aggregates, that involve, in particular, the N-terminal unstructured segment, the apical region including strands S4 and S5 with the connecting loop, and the opposite active site.
先前的研究表明,来自嗜热硫磺酸杆菌的酰基磷酸酶在维持天然结构的条件下,通过形成天然样聚集物的短暂形成,能够形成类淀粉样聚集物。基于先前确定的天然蛋白的 NMR 结构,显示出铁氧还蛋白样折叠和非结构的 N 端片段的特殊存在,我们在这里使用 NMR 光谱在分子水平上表明,当放置在聚集条件下时,嗜热硫磺酸杆菌酰基磷酸酶确实保持天然样构象,并且当蛋白质形成初始聚集物时,至少在低分子量物种中,这种天然样结构仍然存在。基于(1)H 和(15)N 化学位移和氢/氘交换率的联合测量,在不同溶液条件下进行的分析使我们能够在将单体状态转移到聚集条件下以及在形成初始天然样聚集物时监测到最显著的构象变化。在单体蛋白中,观察到整个天然蛋白的氢/氘交换率显著增加,并伴有小的局部结构变化。结果还允许识别天然样聚集物中的分子间相互作用区域,这些区域特别涉及无规卷曲的 N 端未折叠片段、包括 S4 和 S5 链和连接环的顶端区域以及相反的活性位点。