Fig. 9: βarr2 diffusion on CCPs domains. | Nature Communications

Fig. 9: βarr2 diffusion on CCPs domains.

From: Fast-diffusing receptor collisions with slow-diffusing peptide ligand assemble the ternary parathyroid hormone–GPCR–arrestin complex

Fig. 9

A Diffusion coefficient and motion values of βarr2mNG trajectories in the absence and presence of PTH. Data is the mean ± 95% confidence intervals (C.I.) of n = 14/1093 (basal) and n = 26/1032 (PTH) cells/average trajectories of at least N = 3 experiments. **P = 0.0074 by unpaired t-test. BD Scheme illustrating the process of calculating the clathrin-free areas. First, a binary mask was produced from the distribution of CLTAmNG. A Voronoi tessellation diagram was generated from this binary mask. The convergence of vertices in the diagram corresponds to the center of a circle with a radius equal to the distance from a point centered on the farthest edge of a clathrin border (B). The area of the largest empty circle (LEC) and the average of all empty circles were computed (AEC) (C). Data are the mean ± S.E.M. For n = 23/933 cells/average empty circles per cell in 3 independent experiments. Scheme showing a hypothetical molecule recruited to the plasma membrane in the center of a clathrin-empty circle (D). Scheme created in https://BioRender.com. E, F Model of MSD vs time, generated from diffusion values of trajectories for PTH1R and βarr2 in the absence of PTH (E), and PTH1R, βarr2 in presence of PTH and PTHTMR (F). The horizontal discontinued magenta line represents the area of the average empty circles (AEC). The solid lines show when βarr2 and PTH1R (E, F) would reach a clathrin spot in the absence (E) or presence (F) of PTH.

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