posted on 2016-06-18, 00:00authored byRL McAdam, KT Varga, Z. Jiang, FB Young, V. Blandford, PS McPherson, LW Gong, WS Sossin
Synaptotagmin 1 (Syt1) is a synaptic vesicle protein that is important for the kinetics of both exocytosis and endocytosis, and is thus a candidate molecule to link these two processes. Although the tandem Ca(2+)-binding C2 domains of Syt1 have important roles in exocytosis and endocytosis, the function of the conserved juxtamembrane (jxm) linker region has yet to be determined. We now demonstrate that the jxm region of Syt1 interacts directly with the pleckstrin homology (PH) domain of the endocytic protein dynamin 1. By using cell-attached capacitance recordings with millisecond time resolution to monitor clathrin-mediated endocytosis of single vesicles in neuroendocrine chromaffin cells, we find that loss of this interaction prolongs the lifetime of the fission pore leading to defects in the dynamics of vesicle fission. These results indicate a previously undescribed interaction between two major regulatory proteins in the secretory vesicle cycle and that this interaction regulates endocytosis.
Funding
This work was supported by a Natural Sciences and Engineering Research Council
of Canada (NESRC) grant to W.S.S.; a Canadian Institutes of Health Research
[grant number MOP-15396 to P.S.M.]; and a National Science Foundation (NSF) award [grant number 1145581 to L.-W.G.]. W.S.S. and P.S.M. are James McGill
Professors.