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 |
| Klingauf, Jürgen |
Duration: 01/01/2022 - 31/12/2025 | 2nd Funding period Funded by: DFG - Collaborative Research Centre Type of project: Subproject in DFG-joint project hosted at University of Münster |
Duration: 01/01/2026 - 31/12/2029 | 3rd Funding period Funded by: DFG - Collaborative Research Centre Type of project: Main DFG-project hosted at University of Münster |