Fundamentals of Complement System – Part 1


What is a Complement System?

Complement system consists of series of proteins which complement or augment the function of the antibodies and augment the inflammatory reactions.

Where the Complementary proteins are produced?

Complement proteins are produced by the liver or the hepatocytes, some of the complement proteins are produced in GI mucosa. There are more 20 proteins among the complement proteins. They can be defined as inactive proteins or inactive enzymes, which are activated only during inflammatory reaction and immune mediated reactions.

How Complement System is activated?

As soon as antibody (specially IGG and IGM)) bind with antigen it undergoes transformational changes and exposes a special domain which binds and activate the complement system.

Early stage of Complement System

Class of antibody (IGG or IGM ) binds with the antigen which activate complement protein number 1, once it is activated it hydraulically  breaks down the complement number 2 and 4. Complement number 4 is break down into ‘A’ and ‘B’ and similar break down happens to the complement number 2, ‘A’ and ‘B’ remain with the bold chain and complements move away. These similar sequences happen to the complement number C3 and make C5 converters, which has power to break down C5 and convert into active form.

Late events in Complement System

complement systemC5b complex with C5, C6, C7, C8 and C9 make a pentameric pore. This pore acts as a membrane attacking pore and destroy the physical integrity of bacterial lipid membrane. This membrane attacking complex is formed as a result of late events occurred in terminal pathway in complement system. The whole pathway, activation of the complement system is called classical pathway.

The Role C3b in Complement System 

C3b facilitates the phagocytosi of bacteria. Any molecule which facilitate the phagocytosis is called opsonin. The two know opsonin molecules are C3b and IGG