Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2052616 | FEBS Letters | 2006 | 7 Pages |
Abstract
We previously identified two forms of endocytosis using capacitance measurements in chromaffin cells: rapid endocytosis (RE), dynamin-1 dependent but clathrin-independent and slow endocytosis (SE), dynamin-2 and clathrin-dependent. Various recombinant SH3 domains that interact with the proline-rich domain of dynamin were introduced into single cells via the patch pipette. GST-SH3 domains of amphiphysin-1, intersectin-IC, and endophilin-I inhibited SE but had no effect on RE. Grb2-SH3 (N-terminal) or a mutant of amphiphysin-1-SH3 was inactive on either process. These data confirm that dynamin-1 dependent RE is independent of clathrin and show that amphiphysin is exclusively associated with clathrin and dynamin-2-dependent SE.
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Authors
Abdeladim Elhamdani, Fouad Azizi, Elena Solomaha, H. Clive Palfrey, Cristina R. Artalejo,