Immunoglobulins: Structure and Function Aulanni’am Biochemistry Laboratory Faculty of Sciences_UB.

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Presentation transcript:

Immunoglobulins: Structure and Function Aulanni’am Biochemistry Laboratory Faculty of Sciences_UB

Immunoglobulins:Structure and Function Definition: Glycoprotein molecules that are produced by plasma cells in response to an immunogen and which function as antibodies Immune serum Ag adsorbed serum 11 22   + - albumin globulins Mobilit y Amount of protein

General Functions of Immunoglobulins Effector functions  Fixation of complement  Binding to various cells (Usually require Ag binding) Ag binding –Can result in protection

Basic Immunoglobulin Structure Immunoglobulins - heterogeneous Myeloma proteins - homogeneous immunoglobulins

Immunoglobulin Structure Heavy & Light Chains Disulfide bonds  Inter-chain  Intra-chain C H1 VLVL CLCL VHVH C H2 C H3 Hinge Region Carbohydrate Disulfide bond

Immunoglobulin Structure Variable & Constant Regions  V L & C L  V H & C H Hinge Region C H1 VLVL CLCL VHVH C H2 C H3 Hinge Region Carbohydrate Disulfide bond

Immunoglobulin Structure Domains  V L & C L  V H & C H1 - C H3 (or C H4 ) Oligosaccharid es C H1 VLVL CLCL VHVH C H2 C H3 Hinge Region Carbohydrate Disulfide bond

IgG molecule

Structure of the Variable Region Hypervariable (HVR) or complimentarity determining regions (CDR) HVR3 FR1 FR2 FR3 FR4 HVR1 HVR2 Variability Index Amino acid residue Framework regions

Immunoglobulin Fragments: Structure/Function Relationships Fab  Ag binding  Valence = 1  Specificty determined by V H and V L Papain Fc Fab Fc  Effector functions

Immunoglobulin Fragments: Structure/Function Relationships Ag Binding Complement Binding Site Placental Transfer Binding to Fc Receptors

Immunoglobulin Fragments: Structure/Function Relationships Fab  Ag binding Fc  Effector functions F(ab’) 2 Pepsin Fc Peptides F(ab’) 2

Human Immunoglobulin Classes IgG - Gamma (  ) heavy chains IgM - Mu (  ) heavy chains IgA - Alpha (  ) heavy chains IgD - Delta (  ) heavy chains IgE - Epsilon (  ) heavy chains

Human Immunoglobulin Subclasses IgG Subclasses  IgG1 - Gamma 1 (  1) heavy chains  IgG2 - Gamma 2 (  2) heavy chains  IgG3 - Gamma 3 (  3) heavy chains  IgG4 - Gamma 4 (  4) heavy chains IgA subclasses  IgA1 - Alpha 1 (  1) heavy chains  IgA2 - Alpha 2 (  2) heavy chains

Human Immunoglobulin Light Chain Types Kappa (  ) Lambda (  )

Human Immunoglobulin Light Chain Subtypes Lambda light chains  Lambda 1 (  1)  Lambda 2 (  2)  Lambda 3 (  3)  Lambda 4 (  4)

Immunoglobulins Nomenclature  IgM (kappa)  IgA1(lambda 2)  IgG Heterogeneity

IgG Structure  Monomer (7S) IgG1, IgG2 and IgG4IgG3

IgG Structure Properties  Major serum Ig  Major Ig in extravascular spaces  Placental transfer – Does not require Ag binding (  IgG2)  Fixes complement (  IgG4)  Binds to Fc receptors (  IgG2, IgG4) Phagocytes - opsonization K cells - ADCC

IgM Structure  Pentamer (19S)  Extra domain (C H4 )  J chain C4C4 J Chain

IgM Structure Properties  3rd highest serum Ig  First Ig made by fetus and B cells  Fixes complement

Fixation of C1 by IgG and IgM Abs C1r C1s C1q C1r C1s C1q No activationActivation

IgM Structure Properties  3rd highest serum Ig  First Ig made by fetus and B cells  Fixes complement Tail Piece  Agglutinating Ig  Binds to Fc receptors  B cell surface Ig

B Cell Antigen Receptor (BcR) Ig-  Ig- 

IgA Structure  Serum - monomer  Secretions (sIgA) Dimer (11S) J chain Secretory component J ChainSecretory Piece

IgA Structure Properties  2nd highest serum Ig  Major secretory Ig (Mucosal or Local Immunity) Tears, saliva, gastric and pulmonary secretions  Does not fix complement (unless aggregated)  Binds to Fc receptors on some cells

IgD Structure  Monomer  Tail piece Tail Piece

IgD Structure Properties  4th highest serum Ig  B cell surface Ig  Does not bind complement

IgE Structure  Monomer  Extra domain (C H4 ) C4C4

IgE Structure Properties  Least common serum Ig Binds to basophils and mast cells (Does not require Ag binding)  Allergic reactions  Parasitic infections (Helminths) Binds to Fc receptor on eosinophils  Does not fix complement