Target Name: ADAM22
NCBI ID: G53616
Other Name(s): Metalloproteinase-disintegrin ADAM22-3 | EIEE61 | ADAM metallopeptidase domain 22, transcript variant 4 | metalloproteinase-disintegrin ADAM22-3 | Metalloproteinase-like, disintegrin-like, and cysteine-rich protein 2 | DEE61 | Disintegrin and metalloproteinase domain-containing protein 22 (isoform 4) | A disintegrin and metalloproteinase domain 22 | MDC2 | ADAM22 variant 4 | ADA22_HUMAN | metalloproteinase-like, disintegrin-like, and cysteine-rich protein 2 | a disintegrin and metalloproteinase domain 22 | Disintegrin and metalloproteinase domain-containing protein 22 | ADAM metallopeptidase domain 22 | ADAM 22

ADAM22: A Potential Drug Target and Biomarker for Inflammatory Neurodegenerative Diseases

Inflammatory neurodegenerative diseases, such as multiple sclerosis, rheumatoid arthritis, and progressive motor neuron disease, are characterized by the progressive loss of brain cells and the formation of immune complexes, leading to neuroinflammation. These diseases are often treated with immunomodulatory drugs, which aim to reduce the production of immune cells and slow down the progression of neurodegeneration. However, these treatments can be effective only for a limited period of time and may have potential adverse effects. Therefore, there is a need for new drug targets and biomarkers to improve the treatment of inflammatory neurodegenerative diseases.

ADAM22: A Potential Drug Target and Biomarker

The ADAM22 gene, which encodes a protein named Adam22, has been identified as a potential drug target and biomarker for the treatment of inflammatory neurodegenerative diseases. The ADAM22 protein is involved in the regulation of various cellular processes, including cell adhesion, migration, and invasion. It is also involved in the production of immune complexes, which are a hallmark of neuroinflammation. Therefore, targeting the ADAM22 protein could potentially lead to new treatments for inflammatory neurodegenerative diseases.

Drug Targeting of ADAM22

One approach to targeting the ADAM22 protein is to use small molecules, such as inhibitors or modulators, to disrupt its function. Small molecules can be found in natural products, such as herbal extracts, or can be synthesized using various techniques. One such small molecule, called N-acetyl-L-glutamyl-L-serine (N-ACGlu-L-Ser), has been shown to inhibit the ADAM22 protein and reduce the production of immune complexes in mouse models of multiple sclerosis and rheumatoid arthritis.

Biomarker Analysis

To further validate the potential of ADAM22 as a drug target and biomarker, researchers have used various techniques to analyze the expression and distribution of the ADAM22 protein in mouse models of inflammatory neurodegenerative diseases. They have found that the ADAM22 protein is expressed in the brains of patients with multiple sclerosis and rheumatoid arthritis and that its levels are increased in the spinal cord of patients with these diseases. Furthermore, they have shown that the ADAM22 protein is involved in the production of immune complexes and that inhibiting its function can reduce the production of immune cells in these diseases.

Conclusion

In conclusion, ADAM22 is a potential drug target and biomarker for the treatment of inflammatory neurodegenerative diseases. The disruption of ADAM22 function using small molecules or genetic modification could potentially lead to new treatments for these diseases. Further research is needed to validate the effectiveness of ADAM22 as a drug target and biomarker and to develop safe and effective treatments for inflammatory neurodegenerative diseases.

Protein Name: ADAM Metallopeptidase Domain 22

Functions: Probable ligand for integrin in the brain. This is a non catalytic metalloprotease-like protein (PubMed:19692335). Involved in regulation of cell adhesion and spreading and in inhibition of cell proliferation. Neuronal receptor for LGI1

More Common Targets

ADAM23 | ADAM28 | ADAM29 | ADAM30 | ADAM32 | ADAM33 | ADAM3A | ADAM5 | ADAM6 | ADAM7 | ADAM7-AS1 | ADAM7-AS2 | ADAM8 | ADAM9 | ADAMDEC1 | ADAMTS1 | ADAMTS10 | ADAMTS12 | ADAMTS13 | ADAMTS14 | ADAMTS15 | ADAMTS16 | ADAMTS16-DT | ADAMTS17 | ADAMTS18 | ADAMTS19 | ADAMTS2 | ADAMTS20 | ADAMTS3 | ADAMTS4 | ADAMTS5 | ADAMTS6 | ADAMTS7 | ADAMTS7P1 | ADAMTS7P3 | ADAMTS7P4 | ADAMTS8 | ADAMTS9 | ADAMTS9-AS1 | ADAMTS9-AS2 | ADAMTSL1 | ADAMTSL2 | ADAMTSL3 | ADAMTSL4 | ADAMTSL4-AS1 | ADAMTSL5 | ADAP1 | ADAP2 | Adapter protein complex 5 | Adaptor-related protein complex 1 | Adaptor-related protein complex 2 | Adaptor-Related Protein Complex 3 | Adaptor-related protein complex 4 | ADAR | ADARB1 | ADARB2 | ADARB2-AS1 | ADAT1 | ADAT2 | ADAT3 | ADCK1 | ADCK2 | ADCK5 | ADCY1 | ADCY10 | ADCY10P1 | ADCY2 | ADCY3 | ADCY4 | ADCY5 | ADCY6 | ADCY7 | ADCY8 | ADCY9 | ADCYAP1 | ADCYAP1R1 | ADD1 | ADD2 | ADD3 | ADD3-AS1 | Adducin | Adenosine A2 receptor | Adenosine deaminase | Adenosine receptor | Adenylate Cyclase | ADGB | ADGB-DT | ADGRA1 | ADGRA2 | ADGRA3 | ADGRB1 | ADGRB2 | ADGRB3 | ADGRB3-DT | ADGRD1 | ADGRD2 | ADGRE1 | ADGRE2 | ADGRE3 | ADGRE4P