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小 GTPase 活性分析(SAIYAN)系统:一种检测活细胞中 GTPase 激活的方法。

Small GTPase ActIvitY ANalyzing (SAIYAN) system: A method to detect GTPase activation in living cells.

机构信息

Department of Biological Informatics and Experimental Therapeutics, Graduate School of Medicine, Akita University, Akita, Japan.

出版信息

J Cell Biol. 2024 Oct 7;223(10). doi: 10.1083/jcb.202403179. Epub 2024 Aug 5.

Abstract

Small GTPases are essential in various cellular signaling pathways, and detecting their activation within living cells is crucial for understanding cellular processes. The current methods for detecting GTPase activation using fluorescent proteins rely on the interaction between the GTPase and its effector. Consequently, these methods are not applicable to factors, such as Sar1, where the effector also functions as a GTPase-activating protein. Here, we present a novel method, the Small GTPase ActIvitY ANalyzing (SAIYAN) system, for detecting the activation of endogenous small GTPases via fluorescent signals utilizing a split mNeonGreen system. We demonstrated Sar1 activation at the endoplasmic reticulum (ER) exit site and successfully detected its activation state in various cellular conditions. Utilizing the SAIYAN system in collagen-secreting cells, we discovered activated Sar1 localized both at the ER exit sites and ER-Golgi intermediate compartment (ERGIC) regions. Additionally, impaired collagen secretion confined the activated Sar1 at the ER exit sites, implying the importance of Sar1 activation through the ERGIC in collagen secretion.

摘要

小分子 GTPases 在各种细胞信号通路中至关重要,检测其在活细胞内的激活对于理解细胞过程至关重要。目前使用荧光蛋白检测 GTPase 激活的方法依赖于 GTPase 与其效应物的相互作用。因此,这些方法不适用于 Sar1 等因子,因为效应物也作为 GTPase 激活蛋白发挥作用。在这里,我们提出了一种新的方法,即小分子 GTPase ActIvitY ANalyzing(SAIYAN)系统,用于通过荧光信号利用分裂 mNeonGreen 系统检测内源性小分子 GTPase 的激活。我们在内质网(ER)出口位点展示了 Sar1 的激活,并成功在各种细胞条件下检测到其激活状态。在分泌胶原蛋白的细胞中使用 SAIYAN 系统,我们发现激活的 Sar1 定位于 ER 出口位点和内质网-高尔基体中间区(ERGIC)区域。此外,受损的胶原蛋白分泌将激活的 Sar1 局限在 ER 出口位点,这表明通过 ERGIC 激活 Sar1 在胶原蛋白分泌中的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83e5/11303508/e2ca525003c4/JCB_202403179_Fig1.jpg

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