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bioRxiv · 10.1101/2021.09.13.460139

Activation of the adhesion GPCR GPR133 (ADGRD1) by antibodies targeting the N-terminus

Stephan, G.·Frenster, J. D.·Liebscher, I.·Placantonakis, D. G.
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Abstract

We recently demonstrated that GPR133 (ADGRD1), an adhesion G protein-coupled receptor (aGPCR) whose canonical signaling raises cytosolic cAMP, is necessary for growth of glioblastoma (GBM) and is de novo expressed in GBM relative to normal brain tissue. We showed that dissociation of autoproteolytically generated N-terminal and C-terminal fragments (NTF and CTF) of GPR133 at the plasma membrane promotes receptor activation and increases signaling. Toward developing biologics modulating GPR133 function, we tested antibodies against the N-terminus of GPR133 for effects on receptor signaling. Treatment of HEK293T cells overexpressing GPR133 with such antibodies increased cAMP levels in a concentration-dependent manner. Analysis of supernatants following antibody treatment revealed complexes of the antibodies with the autoproteolytically cleaved NTF of GPR133. Cells expressing a cleavage-deficient mutant GPR133 (H543R) did not respond to antibody stimulation, suggesting that the effect is cleavage-dependent. The antibody-mediated stimulation of wild-type GPR133, but not the cleavage-deficient H543R mutant, was reproducible in patient-derived GBM cells. These findings provide a paradigm for modulation of GPR133 function with biologics and support the hypothesis that NTF-CTF dissociation promotes receptor activation and signaling.

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Stephan, G., Frenster, J. D., Liebscher, I., Placantonakis, D. G.. 2021-09-14. Activation of the adhesion GPCR GPR133 (ADGRD1) by antibodies targeting the N-terminus. https://doi.org/10.1101/2021.09.13.460139

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