Institut de Biochimie et Génétique Cellulaires, UMR 5095 University Bordeaux-2 and CNRS, 1 rue Camille St Saëns, 33077, Bordeaux cedex, France.
Naunyn Schmiedebergs Arch Pharmacol. 2011 Oct;384(4-5):373-81. doi: 10.1007/s00210-011-0628-8. Epub 2011 Apr 12.
The human nucleoside diphosphate (NDP) kinase A, product of the NME1 gene also named NM23-H1, is known as a metastasis suppressor protein. A naturally occurring variant, S120G, identified in neuroblastomas, possesses native three-dimensional structure and enzymatic activity but displays reduced conformational stability and a folding defect with the accumulation of a "molten globule" folding intermediate during refolding in vitro. As such intermediate has been postulated to be involved in amyloid formation, NDP kinase A may serve as a model protein for studying the relationship between folding intermediates and amyloid fibrils. The NDP kinase A S120G was heated in phosphate buffer (pH 7.0). The protein precipitated as amyloid fibrils, as demonstrated by electron microscopy, Congo red, and thioflavin T binding and FTIR spectroscopy. The NDP kinase A S120G, at neutral pH and at moderate temperature experiences a transition towards amyloid fibrils. The aggregation process was faster if seeded by preformed fibrils. The fibrils presented a large proteinase K-resistant core not including residue Gly 120, as shown by mass spectrometry. This suggests that the aggregation process is triggered by the reduced stability of the S120G variant and not by a specific increase in the kinase domain intrinsic aggregation propensity at the place of mutation. This constitutes one of the few reports on a protein involved in cancer biology able to aggregate into amyloid structures under mild conditions.
人类核苷二磷酸(NDP)激酶 A,NME1 基因的产物,也称为 NM23-H1,是一种已知的转移抑制蛋白。在神经母细胞瘤中发现了一种天然存在的变异体 S120G,它具有天然的三维结构和酶活性,但显示出较低的构象稳定性和折叠缺陷,在体外重折叠过程中会积累“无定形球蛋白”折叠中间体。由于这种中间体被假定与淀粉样纤维的形成有关,NDP 激酶 A 可能作为研究折叠中间体和淀粉样纤维之间关系的模型蛋白。在磷酸盐缓冲液(pH 7.0)中加热 NDP 激酶 A S120G。如电子显微镜、刚果红和硫黄素 T 结合和傅里叶变换红外光谱所示,该蛋白沉淀为淀粉样纤维。NDP 激酶 A S120G 在中性 pH 和中等温度下经历向淀粉样纤维的转变。如果用预先形成的纤维接种,聚集过程会更快。纤维呈现出一个大的蛋白水解酶抗性核心,不包括残基 Gly 120,如质谱所示。这表明聚集过程是由 S120G 变体的稳定性降低引发的,而不是由于突变部位激酶结构域内在聚集倾向的特异性增加引发的。这是少数关于参与癌症生物学的蛋白质在温和条件下能够聚集形成淀粉样结构的报告之一。