Affiliation:
1. Akita University 1 Department of Biological Informatics and Experimental Therapeutics, Graduate School of Medicine, , Akita, Japan
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.
Funder
Japan Society for the Promotion of Science Grants-in-Aid for Scientific Research
Ministry of Education, Culture, Sports, Science and Technology of Japan
Akita University
Naito Foundation
Takeda Science Foundation
Toray Science Foundation
Sumitomo Foundation
Suzuken Memorial Foundation
Yasuda Medical Foundation
Foundation for Promotion of Cancer Research
Asahi Glass Foundation
Princess Takamatsu Cancer Research Foundation
Japan Foundation for Applied Enzymology
Kato Memorial Bioscience Foundation
Astellas Foundation for Research on Metabolic Disorders
Inamori Foundation
Kao Foundation for Arts and Sciences
Koyanagi Foundation
Publisher
Rockefeller University Press