At the synaptic cellular interface compensatory endocytosis after synaptic vesicle exocytosis is crucial to maintain a pool of release-ready vesicles at predefined release sites. We use our xenapse culture system in conjunction with total internal reflection fluorescence microscopy (TIRFM) and CRISPR-Cas9 genome editing to visualize individual exocytosis and endocytosis events and study the function of release sites and endocytic membrane domains. Cryo-electron tomography of xenapses grown on TEM grids is utilized to correlate function with structure.
| Klingauf, Jürgen | Institute of Medical Physics and Biophysics |
| Klingauf, Jürgen | Institute of Medical Physics and Biophysics |