Takahashi Nozomu, Watanabe Seiji, Wakasugi Keisuke
Department of Life Sciences, Graduate School of Arts and Sciences, The University of Tokyo, Meguro-ku, Tokyo, Japan.
PLoS One. 2013 Dec 23;8(12):e83698. doi: 10.1371/journal.pone.0083698. eCollection 2013.
Mammalian neuroglobin (Ngb) protects neuronal cells under conditions of oxidative stress. We previously showed that human Ngb acts as a guanine nucleotide dissociation inhibitor (GDI) for the α-subunits of heterotrimeric Gi/o proteins and inhibits reductions in cAMP concentration, leading to protection against cell death. In the present study, we created human E60Q Ngb mutant and clarified that Glu60 of human Ngb is a crucial residue for its GDI and neuroprotective activities. Moreover, we investigated structural and functional properties of several human Ngb mutants and demonstrated that the neuroprotective effect of human Ngb is due to its GDI activity and not due to its scavenging activity against reactive oxygen species.
哺乳动物神经球蛋白(Ngb)在氧化应激条件下可保护神经细胞。我们之前表明,人Ngb作为异源三聚体Gi/o蛋白α亚基的鸟嘌呤核苷酸解离抑制剂(GDI),并抑制cAMP浓度降低,从而起到保护细胞免于死亡的作用。在本研究中,我们构建了人E60Q Ngb突变体,并阐明人Ngb的Glu60是其GDI和神经保护活性的关键残基。此外,我们研究了几种人Ngb突变体的结构和功能特性,并证明人Ngb的神经保护作用归因于其GDI活性,而非其对活性氧的清除活性。