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Audet and collaborators found that DOR activated by SNC-80 strongly interacts with arrestin 3 (Audet et al., 2008): when the receptor is phosphorylated by GRK2 and internalized via arrestins it can recycle whereas in a non-phosphorylated form DOR undergoes an arrestin-independent sequestration which is followed by a degradation

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coli as an MBP fusion, resulted in enhanced soluble expression of stable, functional protein [53]

R.et al (2019)

The research above (Badenhorst, Finkley, Abdulghani, Carey/Pickart) all studied topical application