Sr2+ Binding to the Ca2+ Binding Site of the Synaptotagmin 1 C2B Domain Triggers Fast Exocytosis without Stimulating SNARE Interactions
pmid: 12526776
Sr2+ Binding to the Ca2+ Binding Site of the Synaptotagmin 1 C2B Domain Triggers Fast Exocytosis without Stimulating SNARE Interactions
Sr(2+) triggers neurotransmitter release similar to Ca(2+), but less efficiently. We now show that in synaptotagmin 1 knockout mice, the fast component of both Ca(2+)- and Sr(2+)-induced release is selectively impaired, suggesting that both cations partly act by binding to synaptotagmin 1. Both the C(2)A and the C(2)B domain of synaptotagmin 1 bind Ca(2+) in phospholipid complexes, but only the C(2)B domain forms Sr(2+)/phospholipid complexes; therefore, Sr(2+) binding to the C(2)B domain is sufficient to trigger fast release, although with decreased efficacy. Ca(2+) induces binding of the synaptotagmin C(2) domains to SNARE proteins, whereas Sr(2+) even at high concentrations does not. Thus, triggering of the fast component of release by Sr(2+) as a Ca(2+) agonist involves the formation of synaptotagmin/phospholipid complexes, but does not require stimulated SNARE binding.
- Max Planck Society Germany
- The University of Texas Southwestern Medical Center United States
- Max Planck Institute for Multidisciplinary Sciences Germany
Mice, Knockout, Membrane Glycoproteins, Macromolecular Substances, Neuroscience(all), Calcium-Binding Proteins, Presynaptic Terminals, Excitatory Postsynaptic Potentials, Membrane Proteins, Nerve Tissue Proteins, Hippocampus, PC12 Cells, Exocytosis, Protein Structure, Tertiary, Mice, Animals, Newborn, Barium, Animals, Calcium, Calcium Signaling, Phospholipids, Chelating Agents
Mice, Knockout, Membrane Glycoproteins, Macromolecular Substances, Neuroscience(all), Calcium-Binding Proteins, Presynaptic Terminals, Excitatory Postsynaptic Potentials, Membrane Proteins, Nerve Tissue Proteins, Hippocampus, PC12 Cells, Exocytosis, Protein Structure, Tertiary, Mice, Animals, Newborn, Barium, Animals, Calcium, Calcium Signaling, Phospholipids, Chelating Agents
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