Monoclonal Antibodies for Orphan GPCRs in the CNS GPCRs comprise a large family of structurally related membrane proteins with critical functions in neurobiology. As such, they are key therapeutic targets. However, many members of the vast GPCR family remain orphans. A broad range of neurological indications, including schizophrenia, pain, Parkinson's and Alzheimer's diseases, and autism have been linked to orphan GPCRs, making them attractive targets for therapy. The paucity of reagents specific for the orphan GPCRs, however, has stymied drug development. Monoclonal antibodies (MAbs) are known as excellent research tools and have proven to be highly effective therapeutics. However, GPCRs are notoriously difficult antigens against which to raise antibodies, for reasons that include poor immunogenicity, high conservation between species, and a low membrane profile. XORI Corporation has established an innovative platform for rapid identification and optimization of MAbs ex vivo that has the potential to circumvent the challenges presented by GPCRs. The platform has been validated by discovery and optimization of high affinity mAbs (KD<5 nM) against five cell surface proteins, including one GPCR. We propose to generate MAbs against orphan GPCRs that are highly expressed in neurological tissues. Specifically, we will (1) isolate MAbs specific for amino terminal domains of ten orphan GPCRs expressed in the brain, (2) isolate MAbs for ten full length recombinant orphan GPCRs by cell surface selection, and (3) determine functionality of the orphan GPCR monoclonal antibodies by biochemical and cellular characterization. These antibodies will provide invaluable new research tools and will position XORI for Phase II funding to evaluate diagnostic and therapeutic potential in vivo. Phase I deliverable: ten monoclonal antibodies specific for orphan GPCRs and three monoclonal antibodies with orphan GPCR-specific agonistic or antagonistic activity. These MAbs will open doorways to understanding function of the orphan receptors and will have the potential for diagnostic and therapeutic utility. Relevance: G protein-coupled receptors (GPCRs) comprise an important class of drug targets in neurological disease, but a large percentage of them remain poorly understood. We propose to generate monoclonal antibodies against a number of the "orphan" GPCRs using a novel ex vivo antibody discovery technology that circumvents the main challenges to antibody generation specific to GPCRs. These antibodies will provide important research reagents and may have diagnostic and therapeutic utility.
Public Health Relevance: G protein-coupled receptors (GPCRs) comprise an important class of drug targets in neurological disease, but a large percentage of them remain poorly understood. We propose to generate monoclonal antibodies against a number of the "orphan" GPCRs using a novel ex vivo antibody discovery technology that circumvents the main challenges to antibody generation specific to GPCRs. These antibodies will provide important research reagents and may have diagnostic and therapeutic utility.
Public Health Relevance Statement: G protein-coupled receptors (GPCRs) comprise an important class of drug targets in neurological disease, but a large percentage of them remain poorly understood. We propose to generate monoclonal antibodies against a number of the "orphan" GPCRs using a novel ex vivo antibody discovery technology that circumvents the main challenges to antibody generation specific to GPCRs. These antibodies will provide important research reagents and may have diagnostic and therapeutic utility.
NIH Spending Category: Biotechnology; Mental Health; Neurosciences
Project Terms: Affinity; Agonist; Alzheimer's Disease; Antibodies; Antigens; Autistic Disorder; base; Binding (Molecular Function); Biochemical; Biological; Biological Assay; Brain; cell growth; Cell surface; Cell Surface Proteins; Cell Surface Receptors; Cells; Central Nervous System Diseases; Clinical; commercial application; Communities; Crystallization; Diagnostic; Disease; Dissociation; Drug Delivery Systems; drug development; drug discovery; Evaluation; Extracellular Domain; Family; Funding; G-Protein-Coupled Receptors; Generations; Government; Gray unit of radiation dose; human GPRC5C protein; immunogenicity; Immunoglobulin Genes; Immunohistochemistry; in vivo; Individual; innovation; Knockout Mice; Length; Life; Link; Malignant neoplasm of central nervous system; Malignant Neoplasms; member; Membrane; Membrane Proteins; Methods; Molecular; Monoclonal Antibodies; Multiple Sclerosis; neoplastic cell; nervous system disorder; Neurobiology; Neurologic; novel; Orphan; Pain; Parkinson Disease; Pathway interactions; Persons; Phase; Positioning Attribute; Reagent; receptor; Receptor Cell; Recombinants; Research; Schizophrenia; Signal Transduction; small molecule; Specificity; technological innovation; Technology; Therapeutic; therapeutic target; Tissues; tool; tumor
