核糖体组装因子 LSG1 与囊泡相关膜蛋白相关蛋白(VAPs)相互作用

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-01-01 Epub Date: 2024-08-12 DOI:10.1080/10985549.2024.2384600
Putri Sutjita, Sharmishtha Musalgaonkar, Jeffrey Recchia-Rife, Lisa Huang, Blerta Xhemalce, Arlen W Johnson
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引用次数: 0

摘要

LSG1 是一种参与核糖体组装的保守 GTP 酶。它需要将核输出适配器 NMD3 从细胞质中的前 60S 亚基中驱逐出来。在人体细胞中,LSG1 还与主要存在于内质网的囊泡相关膜蛋白相关蛋白(VAPs)相互作用。VAPs 与大量含有 FFAT 矩阵(酸性束中有两个苯丙氨酸 (FF))的蛋白质相互作用,这些蛋白质参与了许多细胞功能,包括膜运输和脂质运输调节。在这里,我们发现人类 LSG1 通过一个非典型的 FFAT 样基序与 VAPs 结合。缺失该基序会特异性地破坏 LSG1 在 ER 中的定位,但不会扰乱细胞中依赖于 LSG1 的 NMD3 循环或体外 LSG1 GTPase 活性的调节。
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The Ribosome Assembly Factor LSG1 Interacts with Vesicle-Associated Membrane Protein-Associated Proteins (VAPs).

LSG1 is a conserved GTPase involved in ribosome assembly. It is required for the eviction of the nuclear export adapter NMD3 from the pre-60S subunit in the cytoplasm. In human cells, LSG1 has also been shown to interact with vesicle-associated membrane protein-associated proteins (VAPs) that are found primarily on the endoplasmic reticulum. VAPs interact with a large host of proteins which contain FFAT motifs (two phenylalanines (FF) in an acidic tract) and are involved in many cellular functions including membrane traffic and regulation of lipid transport. Here, we show that human LSG1 binds to VAPs via a noncanonical FFAT-like motif. Deletion of this motif specifically disrupts the localization of LSG1 to the ER, without perturbing LSG1-dependent recycling of NMD3 in cells or modulation of LSG1 GTPase activity in vitro.

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CiteScore
7.20
自引率
4.30%
发文量
567
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