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. 2017 Apr 28;8:15061. doi: 10.1038/ncomms15061

Figure 5. Step size distribution analysis reveals that the PR domain does not interfere with lipid interactions with N-terminal domains.

Figure 5

The step size distribution was acquired from multiple single molecule diffusion trajectories for (a) SOSCat, (b) SOSCatPR, (c) SOSHDPC, (d) SOSFL on the Ras-modified lipid membrane containing either 3 mol% of 1,2-dioleoyl-sn-glycero-3-phospho-L-serine (DOPS) or PIP2. All data are adequately fit to a two-species diffusion model. The extracted coefficients were shown in the insets. D1 and D2 correspond to diffusion coefficients of the fast and slow mobility species (unit: μm2 s−1). α corresponds to the fraction of the fast species. The N-terminal domains slow SOS mobility on the PIP2 bilayer, presumably due to specific interaction with the Pleckstrin-homology (PH) domain (c,d)33. Lipid composition (in mol%): egg-PC/MCC-DOPE/DOPS or PIP2=94/3/3. Surface density of Ras: ∼1,200 μm−2.