Research and Publications - Department of Biological Sciences

Permanent URI for this collection

https://ir.ua.edu/handle/123456789/2837

Browse

Browsing Research and Publications - Department of Biological Sciences by Author "Agarwal, Shivani"

Now showing 1 - 1 of 1
  • Thumbnail Image
    Item
    A conformational switch driven by phosphorylation regulates the activity of the evolutionarily conserved SNARE Ykt6
    (National Academy of the Sciences, 2021) McGrath, Kaitlyn; Agarwal, Shivani; Tonelli, Marco; Dergai, Mykola; Gaeta, Anthony L.; Shum, Andrew K.; Lacoste, Jessica; Zhang, Yongbo; Wen, Wenyu; Chung, Daayun; Wiersum, Grant; Shevade, Aishwarya; Zaichick, Sofia; van Rossum, Damian B.; Shuvalova, Ludmilla; Savas, Jeffrey N.; Kuchin, Sergei; Taipale, Mikko; Caldwell, Kim A.; Caldwell, Guy A.; Fasshauer, Dirk; Caraveo, Gabriela; Northwestern University; Feinberg School of Medicine; University of Wisconsin Madison; University of Lausanne; University of Alabama Tuscaloosa; University of Toronto; Fudan University; University of Wisconsin Milwaukee; Pennsylvania State University; Penn State Health; University of Alabama Birmingham; University of Pennsylvania
    Ykt6 is a soluble N-ethylmaleimide sensitive factor activating protein receptor (SNARE) critically involved in diverse vesicular fusion pathways. While most SNAREs rely on transmembrane domains for their activity, Ykt6 dynamically cycles between the cytosol and membrane-bound compartments where it is active. The mechanism that regulates these transitions and allows Ykt6 to achieve specificity toward vesicular pathways is unknown. Using a Parkinson's disease (PD) model, we found that Ykt6 is phosphorylated at an evolutionarily conserved site which is regulated by Ca2+ signaling. Through a multidisciplinary approach, we show that phosphorylation triggers a conformational change that allows Ykt6 to switch from a closed cytosolic to an open membrane-bound form. In the phosphorylated open form, the spectrum of protein interactions changes, leading to defects in both the secretory and autophagy pathways, enhancing toxicity in PD models. Our studies reveal a mechanism by which Ykt6 conformation and activity are regulated with potential implications for PD.