A11 Immunoglobulins: IgG and IgM + A12. Immunoglobulins: IgA, IgE and IgD Flashcards
IgG
65-80% of serum Ig-s Molecular weight (Mw): 160000 Da Monomeric, Structure: bivalent γ heavy chain, y-shaped with 4 peptide chains (2 heavy and 2 light) and disulphide bridges, t1/2: 10-20 days Can cross the endothelium
Functions • Agglutination • Precipitation • Complement activation • Neutralisation • Opsonosation • Cytotoxic (CT) reactions • protection from bacteria and viruses
IgM
5-15% of serum Ab-s Mw: 900000 Da Structure: Pentameric, -S-S-, J chain, Light (γ) and heavy (μ) chains. t1/2: 5 days Normaly not cross endothelium
Functions Primary immune response BCR (as monomer) Agglutination Neutralisation Complement activation CT rarely, through complement
IgA
- Makes up 5-10% of serum Igs, on body surfaces, cell membrane.
- T1/2 = 7 days in serum and 2 days on surface.
- Dimeric, mostly monomer in blood.
- Structure: alpha heavy chain, J chain, secretory component.
- MW: 360,000Da.
- Function: Local immune response, agglutination and neutralisation of pathogens,
- tetravalent, very important in the immune function of mucous membranes.
IgE
- Makes up ≤0.5% of serum Igs, on cell membrane.
- T1/2 = 1-2 days.
- Structure: 2 epsilon heavy chains, 2 light chains.
- MW = 200,000 Da
- Functions: Type 1 hypersensitivity (allergy), protozoal and parasite infections, bivalent.
IgD
- Present on B cells
- Monomer, not stable.
- Structure: Delta heavy chain.
- MW: 180,000
- Function: B-cell receptor – signals B cells to become activated.
Memory B-cells
Do not produce antibodies, but transform easily to plasma cells
Immunoglobulin supergene family
= A large protein superfamily that are responsible for relations among cells of the immune system, recognition and specific antigen binding (globular structure, domains)
• B-cell receptor
• T-cell receptor • Antibody • MHC (Major Histocompatibility Complex) • Fc receptors • Hormone receptors • Differentiation markers (clusters), CD4, CD8 etc.) • Others • Sera of animals recovered from infection o In vitro destroy the microorganism o In vivo protect the animal (passive immunity)
Immunoglobulins can be characterised using Electrophoresis (Agarose Gel/SDS) which separates them on the basis of their size. Amino Acid structure, DNA sequencing, Xray crystallography and electron microscope can also be used.