Target Name: PUM3
NCBI ID: G9933
Review Report on PUM3 Target / Biomarker Content of Review Report on PUM3 Target / Biomarker
PUM3
Other Name(s): Minor histocompatibility antigen HA-8 | Pumilio RNA binding family member 3 | protein 5 transactivated by hepatitis B virus X antigen (HBxAg) | Puf-A | minor histocompatibility antigen HA-8 | Penguin homolog | HBV XAg-transactivated protein 5 | PUM3_HUMAN | KIAA0020 | HLA-HA8 | HBV X-transactivated gene 5 protein | Pumilio domain-containing protein KIAA0020 | PEN | Protein 5 transactivated by hepatitis B virus X antigen (HBxAg) | PUF-A | MGC8749 | XTP5 | RP11-526D20.2 | Pumilio homolog 3 | KIAA0020 protein | PUF6 | HA-8 | pumilio RNA binding family member 3 | penguin homolog

Pum3: A Potential Drug Target and Biomarker for Diseases

Pum3, also known as Minor histocompatibility antigen (MHC) HA-8, is a protein that is expressed in a variety of tissues throughout the body, including the skin, hair, nails, and heart. It is a member of the major histocompatibility complex (MHC), which is a group of proteins that play a critical role in immune responses. MHC molecules are responsible for presenting antigens to T cells, which are crucial for cell-mediated immunity.

Pum3 is a 14-kDa protein that is expressed in human tissues at levels of 1-10% of total protein expression. It is localized to the cytoplasm of cells and is mostly involved in the cytoskeleton structure of the cell. Pum3 has been shown to interact with several other proteins, including the transcription factor NF-kappa-B and the protein kinase A灏?1.

Drug Target and Biomarker

Pum3 has been identified as a potential drug target due to its involvement in several diseases, including cancer, neurodegenerative diseases, and autoimmune disorders. Several studies have shown that inhibiting Pum3 can lead to therapeutic effects in animal models of these diseases.

One of the potential therapeutic strategies for Pum3-related diseases is to target the Pum3 protein itself. This can be done using small molecules, antibodies, or other bioconjugates that specifically bind to Pum3. One such approach is the use of inhibitors of the protein kinase A灏?1, which is known to interact with Pum3.

Another approach to targeting Pum3 is to use antibodies that recognize and label the protein. This can be done using monoclonal antibodies (MCAs) that are specific for Pum3. These antibodies can be used to label the protein in live cells or to purify it from cell extracts or body fluids.

Antibodies against Pum3 have been shown to be effective in several animal models of cancer, neurodegenerative diseases, and autoimmune disorders. For example, a single-cell assay revealed that antibodies against Pum3 can effectively reduce the growth of cancer cells. Similarly, a mouse model of neurodegenerative disease showed that antibodies against Pum3 improved cognitive function and reduced neuroinflammation.

Competitive Assay

To further understand the role of Pum3 in these diseases, researchers have used competitive assays to determine the concentration of Pum3 that is required for its activity. These assays involve measuring the activity of a protein or enzyme in the presence of a known concentration of another protein or enzyme.

One such competitive assay is the classic Michaelis-Menten (MM) assay, which is commonly used to study protein-protein interactions. In this assay, one protein is immobilized on a solid support, while the other protein is immobilized in a solution. The ratio of the activity of the two proteins is then determined by measuring the amount of one protein that binds to the other.

Studies have shown that Pum3 can interact with several other proteins, including the transcription factor NF-kappa-B and the protein kinase A灏?1. These interactions can lead to changes in the activity of these proteins, which can in turn affect the function of the cell.

Conclusion

Pum3 is a protein that is expressed in a variety of tissues throughout the body and has been shown to be involved in several diseases, including cancer, neurodegenerative diseases, and autoimmune disorders. Its role in these diseases is not well understood, but several studies have shown that inhibiting Pum3 or its interacting proteins can lead to therapeutic effects. Further research is needed to fully understand the role of Pum3 in these diseases and to develop effective therapies.

Protein Name: Pumilio RNA Binding Family Member 3

Functions: Inhibits the poly(ADP-ribosyl)ation activity of PARP1 and the degradation of PARP1 by CASP3 following genotoxic stress (PubMed:21266351). Binds to double-stranded RNA or DNA without sequence specificity (PubMed:25512524). Involved in development of the eye and of primordial germ cells (By similarity)

The "PUM3 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 PUM3 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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