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Hereditary spastic paraplegia protein spartin is an FK506-binding protein identified by mRNA display

机译:遗传性痉挛性截瘫蛋白斯巴丁是一种通过mRNA显示鉴定的FK506结合蛋白

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Here, we used mRNA display to search for proteins that bind to FK506, a potent immunosuppressant drug, and identified spartin, a hereditary spastic paraplegia protein, from a human brain cDNA library. We demonstrated that FK506 binds to the C-terminal region of spartin and thereby inhibits the interaction of spartin with TIP47, one of the lipid droplet-associated proteins. We further confirmed that FK506 inhibits localization of spartin and its binder, an E3 ubiquitin ligase AIP4, in lipid droplets and increases the protein level of ADRP (adipose differentiation-related protein), which is a regulator of lipid homeostasis. These results strongly suggest that FK506 suppresses the proteasomal degradation of ADRP, a substrate of AIP4, by inhibiting the spartin-TIP47 interaction and thereby blocking the localization of spartin and AIP4 in lipid droplets.
机译:在这里,我们使用mRNA展示来搜索与FK506(一种有效的免疫抑制剂)结合的蛋白质,并从人脑cDNA文库中鉴定了斯巴丁(一种遗传性痉挛性截瘫蛋白质)。我们证明FK506绑定到spartin的C末端区域,从而抑制了spartin与TIP47的相互作用,TIP47是与脂质液滴相关的蛋白质之一。我们进一步证实FK506抑制脂质滴中的spartin及其结合物E3泛素连接酶AIP4的定位,并增加了ADRP(脂肪分化相关蛋白)的蛋白质水平,ADRP是脂质稳态的调节剂。这些结果强烈表明,FK506通过抑制spartin-TIP47相互作用并从而阻止spartin和AIP4在脂质液滴中的定位,抑制了AIP4的底物ADRP的蛋白酶体降解。

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