Journal of Biological Chemistry · 1998 · 27 citations · 40 references
Life SciencesBiochemistryCell BiologyMolecular NeuroscienceProtein-protein InteractionsStructural BiologyG Protein-coupled Receptor SignalingProtein Complex AssemblyProtein DomainsProtein Interaction DomainsProteolytic ProcessingStable Protein ComplexesG-protein-coupled ReceptorsLimited ProteolysisOpsin BiochemistryProteasome AssemblyProtein Binding DomainsProteolytic StabilityReceptorsRegulatory Subunits
The combination of the Ran-binding domain 4 and cyclophilin domains of Ran-binding protein 2 selectively associate with a subset of G protein-coupled receptors, red/green opsins, upon cis-trans prolyl isomerase-dependent and direct modification of opsin followed by association of the modified opsin isoform to Ran-binding domain 4. This effect enhances in vivo the production of functional receptor and generates an opsin isoform with no propensity to self-aggregate in vitro. We now show that another domain of Ran-binding protein 2, cyclophilin-like domain, specifically associates with the 112-kDa subunit, P112, and other subunits of the 19 S regulatory complex of the 26 S proteasome in the neuroretina. This association possibly mediates Ran-binding protein 2 limited proteolysis into a smaller and stable isoform. Also, the interaction of Ran-binding protein 2 with P112 regulatory subunit of the 26 S proteasome involves still another protein, a putative kinesin-like protein. Our results indicate that Ran-binding protein 2 is a key component of a macro-assembly complex selectively linking protein biogenesis with the proteasome pathway and, thus, with potential implications for the presentation of misfolded and ubiquitin-like modified proteins to this proteolytic machinery.
40
Michael J. Matunis, Elias Coutavas, Gerd A. Blobel · The Journal of Cell Biology · 1996 · 1.2K citations · Full text