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TIP-1 has PDZ scaffold antagonist activity

机译:TIP-1具有PDZ支架拮抗剂活性

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摘要

PDZ proteins usually contain multiple protein-protein interaction domains and act as molecular scaffolds that are important for the generation and maintenance of cell polarity and cell signaling. Here, we identify and characterize TIP-1 as an atypical PDZ protein that is composed almost entirely of a single PDZ domain and functions as a negative regulator of PDZ-based scaffolding. We found that TIP-1 competes with the basolateral membrane mLin-7/CASK complex for interaction with the potassium channel Kir 2.3 in model renal epithelia. Consequently, polarized plasma membrane expression of Kir 2.3 is disrupted resulting in pronounced endosomal targeting of the channel, similar to the phenotype observed for mutant Kir 2.3 channels lacking the PDZ-binding motif. TIP-1 is ubiquitously expressed, raising the possibility that TIP-1 may play a similar role in regulating the expression of other membrane proteins containing a type I PDZ ligand.
机译:PDZ蛋白通常包含多个蛋白-蛋白相互作用域,并充当分子支架,这对于细胞极性和细胞信号的产生和维持很重要。在这里,我们确定和表征TIP-1为非典型的PDZ蛋白,它几乎完全由单个PDZ域组成,并充当基于PDZ的脚手架的负调节剂。我们发现TIP-1与基底外侧膜mLin-7 / CASK复合物竞争与模型肾上皮中钾通道Kir 2.3的相互作用。因此,Kir 2.3的极化质膜表达被破坏,导致明显的内体靶向通道,类似于缺乏PDZ结合基序的突变Kir 2.3通道的表型。 TIP-1无处不在,这增加了TIP-1在调节其他含有I PDZ配体的膜蛋白表达中起类似作用的可能性。

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