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ProteoGenix
Recombinant Proteins
Mammalian cells
Elisa, WB
Sialic acid-binding Ig-like lectin 15 (SIGLEC15) is a type I transmembrane protein that belongs to the SIGLEC family of lectins. It is primarily expressed on the surface of osteoclasts, which are specialized cells responsible for bone resorption. SIGLEC15 has been shown to play a crucial role in regulating osteoclast activity and bone homeostasis. In recent years, it has gained attention as a potential drug target for the treatment of bone-related diseases.
SIGLEC15 is a glycoprotein with a molecular weight of approximately 100 kDa. It consists of an extracellular domain, a transmembrane domain, and a cytoplasmic tail. The extracellular domain contains an N-terminal V-set immunoglobulin-like domain, a C2-set immunoglobulin-like domain, and a mucin-like domain. The V-set and C2-set domains are responsible for binding to sialic acid, while the mucin-like domain is involved in cell-cell interactions. The transmembrane domain anchors the protein to the cell membrane, and the cytoplasmic tail contains signaling motifs that mediate intracellular signaling.
SIGLEC15 is a sialic acid-binding lectin, which means it has a high affinity for sialic acid, a sugar molecule found on the surface of cells. It has been shown to interact with sialylated glycoproteins, including osteoactivin and CD24, on the surface of osteoclasts. This interaction leads to the activation of signaling pathways that regulate osteoclast differentiation and activity.
SIGLEC15 has also been found to play a role in the immune response. It has been shown to modulate the production of inflammatory cytokines and regulate the differentiation of immune cells. In addition, SIGLEC15 has been implicated in tumor growth and metastasis, as it is highly expressed on the surface of cancer cells and promotes their invasion and migration.
Due to its crucial role in bone homeostasis and potential involvement in various diseases, SIGLEC15 has emerged as a promising drug target. Inhibiting SIGLEC15 activity could potentially lead to the development of new treatments for bone-related diseases, such as osteoporosis and rheumatoid arthritis. Studies have shown that blocking SIGLEC15 signaling reduces osteoclast activity and bone resorption, suggesting that targeting this protein could be an effective strategy for treating bone disorders.
In addition, targeting SIGLEC15 could also have implications in cancer treatment. As mentioned earlier, SIGLEC15 is highly expressed on the surface of cancer cells and promotes their invasion and metastasis. Inhibiting SIGLEC15 could potentially prevent cancer cells from spreading to other parts of the body, making it a potential therapeutic target for cancer treatment.
In summary, SIGLEC15 is a sialic acid-binding lectin that plays a crucial role in regulating osteoclast activity and bone homeostasis. It is also involved in immune response and has been implicated in cancer growth and metastasis. As a potential drug target, inhibiting SIGLEC15 could have significant implications in the treatment of bone-related diseases and cancer. Further research on the structure and function of SIGLEC15 is needed to fully understand its potential as a therapeutic target.
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