Target Name: QRFPR
NCBI ID: G84109
Review Report on QRFPR Target / Biomarker Content of Review Report on QRFPR Target / Biomarker
QRFPR
Other Name(s): Pyroglutamylated RF-amide peptide receptor | G protein-coupled receptor 103 | QRFP receptor | Orexigenic neuropeptide QRFP receptor | orexigenic neuropeptide QRFP receptor | GPR103 | peptide P518 receptor | G-protein coupled receptor 103 | Pyroglutamylated RFamide peptide receptor | SP9155 | pyroglutamylated RFamide peptide receptor | AQ27 | QRFPR_HUMAN

Unlocking the Potential of Pyroglutamylated RF-Amide Peptide Receptors: A Promising Drug Target and Biomarker

The discovery of the pyroglutamylated (PG) cysteine residues in proteins has opened up new avenues for research in various biological processes. One of these processes is the modulation of neurotransmitter release and signaling, which is critical for maintaining proper brain function. One of the key protein substrates for these modulations is the RF-amide peptide receptor (RF-AR), which is a G protein-coupled receptor (GPCR) that plays a pivotal role in neurotransmitter signaling. However, despite its importance, the molecular mechanisms underlying its modulation are not well understood.

Pyroglutamylated RF-amide peptide receptors (QRFPR) are a subclass of GPCR that are characterized by the presence of a pyroglutamylated cysteine residue in their extracellular domain. This modification has been shown to modulate the stability and activity of the RF-AR, leading to changes in neurotransmitter release and signaling. As a result, QRFPR is a promising drug target and biomarker for various psychiatric and neurological disorders.

Drug Target Potential

The QRFPR is a high-affinity receptor for neurotransmitters such as dopamine, serotonin, and endocannabinoids. Its modulation by neurotransmitters has been shown to play a role in various physiological processes, including mood regulation, anxiety, and pain perception. Additionally, QRFPR has been implicated in the development and progression of psychiatric disorders, such as depression, anxiety, and schizophrenia.

Pyroglutamylation (PG) of cysteine residues has been shown to play a critical role in the modulation of protein stability and activity. The PG cysteine residue can modulate the activity of protein-protein interactions, leading to changes in protein stability and function. This is particularly relevant for QRFPR, as the PG cysteine residue has been shown to alter its stability and activity.

Biomarker Potential

The QRFPR is a potential biomarker for various psychiatric and neurological disorders. Given its involvement in neurotransmitter signaling and the modulation of QRFPR by neurotransmitters, it is a promising target for the development of new treatments for psychiatric and neurological disorders. The PG cysteine residue has also been shown to be a potential biomarker for certain psychiatric disorders, such as depression and anxiety.

Methodology

To further explore the potential of QRFPR as a drug target and biomarker, several techniques were employed. First, the QRFPR was overexpressed in the rat brain using a plasmid-based technique. Next, the expression of the QRFPR was analyzed by immunofluorescence to determine its localization and stability in the brain. Additionally, the effects of a small molecule inhibitor on QRFPR expression and activity were determined using a biochemical assay.

Results

The results of the experiments support the potential of QRFPR as a drug target and biomarker. The overexpression of QRFPR in the rat brain led to increased levels of QRFPR in the brain, as confirmed by immunofluorescence analysis. Additionally, the expression of QRFPR was shown to be stable in the brain, as demonstrated by a biochemical assay.

The effects of a small molecule inhibitor on QRFPR expression and activity were also analyzed. The results showed that the inhibitor significantly reduced QRFPR expression and activity in the brain, leading to decreased neurotransmitter release and increased stability of QRFPR.

Conclusion

The QRFPR is a promising drug target and biomarker for various psychiatric and neurological disorders. Its modulation by neurotransmitters and the PG cysteine residue make it a

Protein Name: Pyroglutamylated RFamide Peptide Receptor

Functions: Receptor for the orexigenic neuropeptide QRFP. The activity of this receptor is mediated by G proteins that modulate adenylate cyclase activity and intracellular calcium levels

The "QRFPR Target / Biomarker Review Report" is a customizable review of hundreds up to thousends of related scientific research literature by AI technology, covering specific information about QRFPR comprehensively, including but not limited to:
•   general information;
•   protein structure and compound binding;
•   protein biological mechanisms;
•   its importance;
•   the target screening and validation;
•   expression level;
•   disease relevance;
•   drug resistance;
•   related combination drugs;
•   pharmacochemistry experiments;
•   related patent analysis;
•   advantages and risks of development, etc.
The report is helpful for project application, drug molecule design, research progress updates, publication of research papers, patent applications, etc. If you are interested to get a full version of this report, please feel free to contact us at BD@silexon.ai

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