Super-complexes of adhesion GPCRs and neural guidance receptors
| Autor: | Jackson, Verity A., Mehmood, Shahid, Chavent, Matthieu, Roversi, Pietro, Carrasquero, Maria, del Toro, Daniel, Seyit-Bremer, Goenuel, Ranaivoson, Fanomezana M., Comoletti, Davide, Sansom, Mark S. P., Robinson, Carol V., Klein, Rüdiger, Seiradake, Elena |
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| Jazyk: | angličtina |
| Rok vydání: | 2016 |
| Předmět: |
Mice
Knockout Membrane Glycoproteins Receptors Peptide Sequence Homology Amino Acid Science Molecular Sequence Data Receptors Cell Surface Molecular Dynamics Simulation Surface Plasmon Resonance Crystallography X-Ray Article Mass Spectrometry Protein Structure Secondary Protein Structure Tertiary Receptors G-Protein-Coupled HEK293 Cells Multiprotein Complexes Cell Adhesion Animals Humans Amino Acid Sequence Protein Multimerization HeLa Cells Protein Binding |
| Zdroj: | Nature Communications, Vol 7, Iss 1, Pp 1-13 (2016) Nature Communications 'Nature Communications ', vol: 7, pages: 11184-1-11184-13 (2016) |
| ISSN: | 2041-1723 |
| Popis: | Latrophilin adhesion-GPCRs (Lphn1–3 or ADGRL1–3) and Unc5 cell guidance receptors (Unc5A–D) interact with FLRT proteins (FLRT1–3), thereby promoting cell adhesion and repulsion, respectively. How the three proteins interact and function simultaneously is poorly understood. We show that Unc5D interacts with FLRT2 in cis, controlling cell adhesion in response to externally presented Lphn3. The ectodomains of the three proteins bind cooperatively. Crystal structures of the ternary complex formed by the extracellular domains reveal that Lphn3 dimerizes when bound to FLRT2:Unc5, resulting in a stoichiometry of 1:1:2 (FLRT2:Unc5D:Lphn3). This 1:1:2 complex further dimerizes to form a larger ‘super-complex' (2:2:4), using a previously undescribed binding motif in the Unc5D TSP1 domain. Molecular dynamics simulations, point-directed mutagenesis and mass spectrometry demonstrate the stability and molecular properties of these complexes. Our data exemplify how receptors increase their functional repertoire by forming different context-dependent higher-order complexes. FLRT proteins are known to interact with Lphns and Unc5s, mediating cell adhesion and repulsion respectively. Here the authors use crystallography, native mass spectrometry, molecular dynamics simulations and cell-based assays to show that these three proteins form large super-complexes with functions distinct from their smaller subcomplexes. |
| Databáze: | OpenAIRE |
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