Fig. 5: TM1MOR suppresses both MOR and DOR homodimerization. | Nature Communications

Fig. 5: TM1MOR suppresses both MOR and DOR homodimerization.

From: Single-molecule methods for characterizing receptor dimers reveal metastable opioid receptor homodimers that induce functional modulation

Fig. 5

a Schematic figure showing the experimental design for examining the interaction (binding) of TM1MOR with itself, MOR, and DOR. Colocalization indexes (b) and distributions of colocalization durations (c) showing that TM1MOR forms metastable dimers with both MOR and DOR, while the control TM peptide (TMLDLR) shows no interaction with either receptor, suggesting that TM1MOR might be involved in MOR-MOR homodimerization as well as MOR-DOR heterodimerization42. d Schematic figure showing the experimental design for examining whether TM1MOR can suppress homodimerizations of MOR and DOR. e TM1MOR suppresses homodimerization of both MOR and DOR, but not KOR. In contrast, Mpep, Dpep, and Kpep selectively inhibit the homodimerization of MOR, DOR, and KOR, respectively. TMLDLR hardly affects any OR homodimerization. In the box plots (b, e), horizontal bars, crosses, boxes, and whiskers indicate median values, mean values, interquartile ranges (25–75%), and 10-90% ranges, respectively. * and ns represent significant (p < 0.05) and non-significant (p ≥ 0.05) differences, respectively (Tukey’s multiple comparison test). All of the statistical parameters and analysis results including sample size n and p values are provided in Supplementary Data 2. Source data are provided as a Source Data file.

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