Detecting the Activation of Endogenous Small GTPases via Fluorescent Signals Utilizing a Split mNeonGreen: Small GTPase ActIvitY ANalyzing (SAIYAN) System:https://t.co/e1q5j0J8zS
@cell_club I’m excited to share that our research is now published in Nature Communications! Thank you to everyone involved in this work!☺️
@NatureComms#TANGO1#ER_exit_site
Great topic! The phosphorylation-coupled autoregulation of TANGO1 and Sec16A is indeed crucial for maintaining functional ER exit sites. This dynamic process facilitates efficient protein secretion. I'm curious, do you think this mechanism might serve as a potential target for therapeutic intervention in diseases linked to ER stress or protein misfolding?
For comprehensive insights and recent biomedical studies, you might want to check out https://t.co/4Y9Imt8uIJ, a platform that can generate detailed biomedical reviews. #CellBiology #Medicine
🚨 New finding!
How are dynamic ER exit sites (ERES) maintained? 🤔
Our new preprint reveals a phosphorylation-coupled autoregulatory system🔁 that sustains ERES function.
Now on bioRxiv: https://t.co/9Yge7wL3tx
This system allows us to visualize Sar1, which binds to the ER membrane when activated, using split mNeonGreen. We demonstrated that activated Sar1 localizes to the ERGIC with Sec23 during collagen secretion, suggesting its crucial role in this process.
We are excited to announce that our paper on the “SAIYAN” method for visualizing the activation state of small GTPases has been published today in the Journal of Cell Biology!
Miharu Maeda, Kota Saito et al. @syudaikouhou 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. https://t.co/tgkUGfbDjm
We are pleased to share our work on a distant TANGO1 ortholog in C. elegans. A collaboration between Jimmy Mo @oM_ymmiJ, Kwangsek Jung, Yan Li in my lab @hkust and Chao Zhai, Yonghong Yan in Meng-Qiu Dong's lab at NIBS. https://t.co/2AOJCggGsl
Our latest paper! A promising avenue for therapeutic intervention in fibroses, characterized by excessive ECM production, via targeted inhibition of TANGO1-mediated ER export.
TANGO1 inhibitors reduce collagen secretion and limit tissue scarring
https://t.co/BRx36aVhfF
Spotlight: Saito and Maeda discuss work by Yang et al. @PastorParejaLab (https://t.co/D7E0QaZtwC) showing that all four p24 subfamilies are required for secretion and their interactions with Tango1 are vital for a stable ER–Golgi interface. https://t.co/sBKPtyxXb6
This method can be utilized for other small GTPases! Moreover, we also reveal that the localization of activated Sar1 during collagen secretion is distinctive. Please check it out!
This is my first post. I work on ER-Golgi trafficking at Kota Saito’s lab. We recently published a new preprint on BioRxiv. We successfully visualized the activation of Sar1 in cells using a new method. https://t.co/CI7SBUIvfH