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100ug, 1MG
ProteoGenix
Recombinant Proteins
Monoclonal Antibody
XtenCHO
Ebribafusp Biosimilar, also known as Anti-C3 fusion protein, is a therapeutic protein that has been developed as a biosimilar to the original drug, eculizumab. This biosimilar has been designed to target the complement protein C3, which plays a crucial role in the immune system. In this article, we will discuss the structure, activity, and potential applications of Ebribafusp Biosimilar as a therapeutic protein.
Ebribafusp Biosimilar is a fusion protein composed of two different components – a humanized monoclonal antibody and a human complement factor H. The monoclonal antibody portion is derived from eculizumab, while the complement factor H is a natural protein found in the human body. The two components are linked together through a flexible linker, resulting in a single molecule with a molecular weight of approximately 160 kDa.
The monoclonal antibody component of Ebribafusp Biosimilar is made up of two heavy chains and two light chains, which are connected by disulfide bonds. The heavy chains consist of four constant domains (CH1, CH2, CH3, and CH4) and one variable domain (VH), while the light chains have two constant domains (CL) and one variable domain (VL). The variable domains are responsible for binding to the target protein, C3, while the constant domains provide stability and effector functions.
The complement factor H component of Ebribafusp Biosimilar is composed of 20 short consensus repeat (SCR) domains, which are responsible for binding to C3 and regulating its activity. The fusion of complement factor H to the monoclonal antibody allows for enhanced binding and regulation of C3, resulting in a more potent and effective therapy.
Ebribafusp Biosimilar works by binding to C3 and inhibiting its activity. C3 is a key protein in the complement system, which is part of the innate immune response. When activated, C3 triggers a cascade of reactions that result in the destruction of foreign invaders and damaged cells. However, in certain diseases, such as paroxysmal nocturnal hemoglobinuria (PNH) and atypical hemolytic uremic syndrome (aHUS), the complement system is overactive and can cause damage to healthy cells.
By binding to C3, Ebribafusp Biosimilar prevents its activation and subsequent downstream effects. This results in the inhibition of the complement system and reduces the damage to healthy cells. Additionally, the fusion of complement factor H to the monoclonal antibody component of Ebribafusp Biosimilar allows for enhanced regulation of C3, providing a more targeted and effective therapy.
Ebribafusp Biosimilar has been developed as a potential treatment for PNH and aHUS, both of which are rare and life-threatening diseases caused by an overactive complement system. These diseases are characterized by the destruction of red blood cells, leading to anemia, blood clots, and damage to vital organs. By inhibiting the complement system, Ebribafusp Biosimilar can help reduce the symptoms and improve the quality of life for patients with PNH and aHUS.
In addition to its potential use in PNH and aHUS, Ebribafusp Biosimilar may also have applications in other complement-mediated diseases, such as age-related macular degeneration and C3 glomerulopathy. These diseases are also caused by an overactive complement system and could potentially benefit from treatment with Ebribafusp Biosimilar.
In summary, Ebribafusp Biosimilar is a fusion protein composed of a humanized monoclonal antibody and a human complement factor H. It works by binding to the complement protein C3 and inhibiting its activity, resulting in the inhibition of the complement system. This biosimilar has potential applications in rare and life-threatening diseases, such as PNH and aHUS, and may also have
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