SNARE proteins are the core of the cell's fusion machinery and mediate virtually all known intracellular membrane fusion reactions on which exocytosis and trafficking depend. Fusion is catalyzed when vesicle-associated v-SNAREs form trans-SNARE complexes ("SNAREpins") with target membrane-associated t-SNAREs, a zippering-like process releasing ∼65 kT per SNAREpin. Fusion requires several SNAREpins, but how they cooperate is unknown and reports of the number required vary widely. To capture the collective behavior on the long timescales of fusion, we developed a highly coarse-grained model that retains key biophysical SNARE properties such as the zippering energy landscape and the surface charge distribution. In simulations the ∼65-kT zippering energy was almost entirely dissipated, with fully assembled SNARE motifs but uncomplexed linker domains. The SNAREpins self-organized into a circular cluster at the fusion site, driven by entropic forces that originate in steric-electrostatic interactions among SNAREpins and membranes. Cooperative entropic forces expanded the cluster and pulled the membranes together at the center point with high force. We find that there is no critical number of SNAREs required for fusion, but instead the fusion rate increases rapidly with the number of SNAREpins due to increasing entropic forces. We hypothesize that this principle finds physiological use to boost fusion rates to meet the demanding timescales of neurotransmission, exploiting the large number of v-SNAREs available in synaptic vesicles. Once in an unfettered cluster, we estimate ≥15 SNAREpins are required for fusion within the ∼1-ms timescale of neurotransmitter release.SNARE | membrane fusion | exocytosis | entropic force | neurotransmitter release E xocytosis and trafficking in cells depend on membrane fusion reactions, almost all of which are mediated by SNARE proteins (1-3). Fusion is catalyzed by the assembly of vesicleassociated v-SNAREs and target membrane-associated t-SNAREs into coiled coils of α-helices to form trans-SNARE complexes ("SNAREpins"). Assembly initiates at the N-terminal ends of the SNARE motifs and propagates toward the C-terminal transmembrane domains (TMDs) in a zipper-like fashion, pulling the membranes into close proximity and triggering fusion by a mechanism that remains poorly understood.An unanswered question is how SNARE proteins deliver the energy required to fuse membranes, estimated to be ∼40-140 kT (4-6). A common view is that the ∼65 kT per SNAREpin released during zippering (7) provides the necessary energy, but how this is coupled to the membranes is unclear given that the uncomplexed v-SNARE is largely unstructured and presumably flexible (8). It has been proposed that the linker domains (LDs) connecting the SNARE motifs to the TMDs are stiff, so that some zippering energy could be stored as LD bending energy that could deform and fuse membranes (3, 9). Such an effect would presumably be abolished by even a single flexible region. However, EPR spectroscopy suggests linkers are partial...