Table 2.
(A) Dimer stability: wild-type and syb2 mutant SNARE complexes were purified by size exclusion and analyzed by MALLS or analytical ultracentrifugation. [NaCl] at which SNARE complexes are 50% monomeric is taken from Figure 4c. (B) Monomer stability: SNARE complexes were subjected to differential scanning calorimetry to obtain melting point temperatures (Figure 3e). ΔH is based on integration of the melting point transition, whereas ΔHVH is based on peak width and is independent of protein concentration.