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TIP47在Rab9依赖的甘露糖6-磷酸受体运输中的功能纯化与分析

Purification and analysis of TIP47 function in Rab9-dependent mannose 6-phosphate receptor trafficking.

作者信息

Burguete Alondra Schweizer, Sivars Ulf, Pfeffer Suzanne

出版信息

Methods Enzymol. 2005;403:357-66. doi: 10.1016/S0076-6879(05)03031-4.

Abstract

TIP47 (tail interacting protein of 47 kDa) is a cytosolic protein that is essential for the transport of mannose 6-phosphate receptors (MPRs) from endosomes to the trans-Golgi. This protein is recruited from the cytosol onto the surface of late endosomes by Rab9 GTPase, which enables TIP47 to bind to MPR cytoplasmic domains with enhanced affinity. A mutation in a deep hydrophobic cleft of TIP47 (F(236)C) confers enhanced affinity binding to MPR cytoplasmic domains and stabilizes MPRs in living cells. We describe the purification of native and recombinant TIP47 proteins and assays that we use to monitor the function of this protein in MPR transport in living cells.

摘要

TIP47(47 kDa尾部相互作用蛋白)是一种胞质蛋白,对于甘露糖6-磷酸受体(MPRs)从内体转运至反式高尔基体至关重要。该蛋白通过Rab9 GTP酶从胞质溶胶募集到晚期内体表面,这使得TIP47能够以增强的亲和力结合MPR细胞质结构域。TIP47一个深疏水裂缝中的突变(F(236)C)赋予其与MPR细胞质结构域更强的亲和力,并在活细胞中稳定MPRs。我们描述了天然和重组TIP47蛋白的纯化方法以及用于监测该蛋白在活细胞MPR转运中功能的检测方法。

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