Quantitative single-molecule analysis of assembly and Ca²⁺-dependent disassembly of synaptotagmin oligomers on lipid bilayers.

ABSTRACT: Synaptotagmin-1 (Syt-1) self-assembles into ring-like oligomers, and genetic and biochemical evidence suggest that oligomerization is needed to clamp synaptic vesicles and stabilize them for Ca²⁺-evoked release. However, oligomerization has not yet been demonstrated on lipid bilayers or studied in quantitative biophysical terms. Here we utilize single-molecule imaging methods to monitor the assembly and disassembly of oligomeric clusters of Syt-1 on lipid bilayers in real-time. Syt-1 assembled into two distinct classes of oligomers, small (5 ± 2 subunits) and large (15 ± 2 subunits). Each class assembled at a constant k_on that was always proportional to its ultimate size, but both classes disassembled at the same unit rate (k_off) independent of its size. Bo

SUBMITTER: Li F 

PROVIDER: S-EPMC11615320 | biostudies-literature | 2024 Dec

REPOSITORIES: biostudies-literature