[HTML][HTML] A single C2 domain from synaptotagmin I is sufficient for high affinity Ca2+/phospholipid binding.

BA Davletov, TC Südhof - Journal of Biological Chemistry, 1993 - Elsevier
BA Davletov, TC Südhof
Journal of Biological Chemistry, 1993Elsevier
Synaptotagmin I is a Ca (2+)-and phospholipid-binding protein of synaptic vesicles with an
essential function in neurotransmission. Ca2+/phospholipid binding by synaptotagmin I may
be mediated by its C2 domains, sequence motifs that have been implicated in the Ca2+
regulation of a variety of proteins. However, it is currently unknown if C2 domains are
sufficient for Ca2+/phospholipid binding or if they even directly participate in
Ca2+/phospholipid binding. In order to address this question, we have studied the …
Synaptotagmin I is a Ca(2+)- and phospholipid-binding protein of synaptic vesicles with an essential function in neurotransmission. Ca2+/phospholipid binding by synaptotagmin I may be mediated by its C2 domains, sequence motifs that have been implicated in the Ca2+ regulation of a variety of proteins. However, it is currently unknown if C2 domains are sufficient for Ca2+/phospholipid binding or if they even directly participate in Ca2+/phospholipid binding. In order to address this question, we have studied the Ca2+/phospholipid-binding properties of the first C2 domain of synaptotagmin I. Our results show that this C2 domain by itself binds Ca2+ and phospholipids with high affinity (half-maximal binding at 4-6 microM free Ca2+) and exhibits strong positive cooperativity. The C2 domain is specific for negatively charged phospholipids and for those divalent cations that are known to stimulate synaptic vesicle exocytosis (Ca2+ > Sr2+, Ba2+ > Mg2+). These studies establish that C2 domains can serve as independently folding Ca2+/phospholipid-binding domains. Furthermore, the cation specificity and the cooperativity of Ca2+ binding by the C2 domain from synaptotagmin I support a role for this protein in mediating the Ca2+ signal in neurotransmitter release.
Elsevier