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首页> 外文期刊>Journal of Molecular Biology >The NOXO1β PX domain preferentially targets PtdIns(4,5)P 2 and PtdIns(3,4,5)P 3
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The NOXO1β PX domain preferentially targets PtdIns(4,5)P 2 and PtdIns(3,4,5)P 3

机译:NOXO1βPX域优先靶向PtdIns(4,5)P 2和PtdIns(3,4,5)P 3

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摘要

NOXO1β [NOXO1 (Nox organizer 1) β] is a cytosolic protein that, in conjunction with NOXA1 (Nox activator 1), regulates generation of reactive oxygen species by the NADPH oxidase 1 (Nox1) enzyme complex. NOXO1β is targeted to membranes through an N-terminal PX (phox homology) domain. We have used NMR spectroscopy to solve the structure of the NOXO1β PX domain and surface plasmon resonance (SPR) to assess phospholipid specificity. The solution structure of the NOXO1β PX domain shows greatest similarity to that of the phosphatidylinositol 3-kinase-C2α PX domain with regard to the positions and types of residues that are predicted to interact with phosphatidylinositol phosphate (PtdInsP) head groups. SPR experiments identify PtdIns(4,5)P 2 and PtdIns(3,4,5)P 3 as preferred targets of NOXO1β PX. These findings contrast with previous lipid overlay experiments showing strongest binding to monophosphorylated PtdInsP and phosphatidylserine. Our data suggest that localized membrane accumulation of PtdIns(4,5)P 2 or PtdIns(3,4,5)P 2 may serve to recruit NOXO1β and activate Nox1.
机译:NOXO1β[NOXO1(NOx组织者1)β]是一种胞浆蛋白,与NOXA1(NOx激活剂1)共同调节NADPH氧化酶1(Nox1)酶复合物产生的活性氧。 NOXO1β通过N末端PX(phox同源性)结构域靶向膜。我们已经使用NMR光谱法解决了NOXO1βPX域的结构和表面等离振子共振(SPR),以评估磷脂的特异性。关于预测与磷脂酰肌醇磷酸酯(PtdInsP)头基相互作用的残基的位置和类型,NOXO1βPX结构域的溶液结构与磷脂酰肌醇3-激酶-C2αPX结构域显示出最大相似性。 SPR实验确定PtdIns(4,5)P 2和PtdIns(3,4,5)P 3是NOXO1βPX的首选目标。这些发现与以前的脂质覆盖实验相反,脂质实验显示与单磷酸化的PtdInsP和磷脂酰丝氨酸的结合最强。我们的数据表明,PtdIns(4,5)P 2或PtdIns(3,4,5)P 2的局部膜积累可能有助于募集NOXO1β和激活Nox1。

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