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Immunoglobulins - Serum proteins are against a number of important bacterial infections. Introduction All vertebrates possess immunoglobulin-like molecules. Immunoglobulins are synthesized and secreted by end cells of the B cell lineage, i.e. plasma cell.
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Immunoglobulins- Serum proteins are against a number of important bacterial infections. Introduction • All vertebrates possess immunoglobulin-like molecules. • Immunoglobulins are synthesized and secreted by end cells of the B cell lineage, i.e. plasma cell. • Immunoglobulins are largely confined to the broad and heterogeneous band of -globulins and show considerable diversity of structure and function.
Untreated antiserum Treated antiserum • The first evidence to show antibody is one of serum protein fractions • 1939, A. Tiselius and E. A. Kabat • To immunize rabbits with ovalbumin • Belong to -globulin fractionimmunoglobulin
Structure of Immunoglobulins • The typical immunoglobulin molecule is • Asymmetrically composed of four polypeptide chains • Linked by disulphide bridges • The larger chains are designated heavy(MW about 50~77 kDa) and the smaller light (MW about 25 kDa). • The two most important of their features in the immune response are specificity and biologic activity. • Several immunoglobulin fragments can be prepared using proteolytic enzymes and these have been of value in unravelling the functional activities of different parts of these molecules
Papain digestion: • To cleave on the amino-terminal side of the inter-heavy chain disulphide bonds. • To yield two Fab(Fragment antigen-binding)fragments and one Fc(Fragment crystallizable)fragment. • Pepsin digestion : • To cleave on the carboxy-terminal side of the inter-heavy chain disulphide bonds. • To yield a Fab dimer(F(ab' )2)and a rather smaller Fc fragment(pFc')
A MW of 150,000 Da A MW of 100,000 Da A MW of 25,000 Da A MW of 45,000 Da A MW of 50,000 Da A MW of 50,000 Da
The immunoglobulin molecules are in Y configuration and have the flexible hinge region which permits considerable movement of the Fab arms. • Both light and heavy polypeptide chains consist of a series of similar subunits, designated domains. • 每一個domain約由110 amino acids及a single intrachain disulphide bridge堆疊而成之polypeptide chain。 • Light and heavy polypeptide chains之amino-terminal domain的氨基酸組成有較高之變化性,稱為variable region(可變區);和可變區相較之下氨基酸組成變化低的domain,稱為constant region(不可變區)。 • light chain具有單一可變區及不可變區domains(VL及CL);heavy chain具有單一可變區及三到四個不可變區domains (VH及CH1、CH2、CH3、CH4,其不可變區domain數目依immunoglobulin種類而定)。
Ribbon representation of an intact monoclonal antibody depicting the heavy and light chain
Qutternary structure immunoglobulin and interactions between domains • Extended peptide sequence between CH1 and CH2 of , , and heavy chain • Poline rich sequence • Giving IgG, IgD and IgA segmental flexibility
Variable region為immunoglobulin與抗原接觸的部位(antigen-binding site),其中具有三區hot spots (hypervariable regions,HVR1、HVR2、HVR3 or complementarity-determining regions, CDR1、CDR2、CDR3)。 • Affinity: the strength of binging or association of a single epitope for a single combining site • Avidity: indicate the average strength of binding
Diagram of an immunoglobulin light chain depicting the fold structure Held teogether by hydrophobic interaction and disulfide bond
Antigenic Deteminants on Immunoglobulin • Antibodies also are potent immunogens to induce an antibody response • Anti-Ig antibodies are powerful tools • Antigenic determinants (epitopes) on Ig: • Isotypic determinant: constant-region determinants, to distinguish each Ig class and subclass within a species • Allotypic determinant: be able to distinguish the subtle amino acid difference between the same set of isotype genes • Idiotypic determinant: be generated by conformation of amino acid sequences of heavy- and light-chain variable regions specific for each antigen
Individual determinant is called an idiotope. • The sum of the individual idiotope is the idiotype
The Classes and Subclasses of Immunoglobulins • 利用heavy chain constant region的結構和功能的不同可將Immunoglobulins分為IgG、IgA、IgM、IgD、IgE等五類;其中IgG及IgA具有subclasses。
IgG、IgD、IgE為monomer;IgA為dimer;IgM為pentamer。 • J chain: • A small acidic protein,15 kDa,其結構與light and heavy chain無關。 • 由plasma cell分泌而來。 • J chain is disulfide-bonded to the penultimate cysteine residue in the tail piece of theαorμchain。主要用來聚合immunoglobulin monomer。 • Secretory component: • A single polypeptide,about 70 kDa,僅可與IgA聚合在一起;由黏膜皮層細胞產生,這些細胞會將血液中的IgA抓住,使其與secretory component結合後轉移進入分泌系統。 • 其結構中具有高量的carbohydrate;氨基酸組成和 J chain及immunoglobulins沒有相似處。 • 利用非共價鍵的接出方式與游離或被鍵結的IgA相接。
IgG • 具有γ1、γ2、γ3、γ4 四種heavy chains,κ或λlight chain;因此有IgG1(60-70%)、IgG2(14-20%)、IgG3(4-8%)、IgG4(2-6%)四種次種。 • IgG accounts for about 75-80% of the total serum immunoglobulin in normal adult and is the abundant antibody produced during secondary humoral immune responses in the blood。 • IgG1、IgG2、IgG3可活化classical complement pathway,IgG2可額外活化alternative complement pathway。
IgM • 具有μheavy chain,κ或λlight chain。 • 為pentamer,具有10 antigen-binding sites,五個單元由一個J chain連結在一起。 • 重鏈具有四個constant regions。 • IgM accounts for only about 10% of serum immunoglobulin,is the key immunoglobulin of the primary response and an efficient activator of the classical complement pathway,and is the most common immunoglobulin expressed on the surfaces of B cells。 • 因為分子很大,無法由循環系統進入組織液中,但因其對poly-Ig recoptor有高親和性,因此在IgA deficiency時會出現在分泌系統中與secretory piece連結扮演IgA的角色。
IgA • 具有α1、α2兩種heavy chains,κ或λlight chain;因此有IgA1、IgA2(兩者存在的比例為5:1)兩種次種。 • 釋出時為dimer (secretory IgA, 最多可為pentamer)加上secretory component游離於組織及血液中,其間具有J chain連接;如果為membrane-bound form則為monomer。
IgA accounts for only about 10-15% of serum immunoglobulin • The major immunoglobulin of external secretions • The most abundant antibody class was found in saliva, tear, intestinal mucus, bronchial secretions, milk, prostatic fluid, and other secretions。 • 不會活化classical complement pathway,但可以協助alternative complement pathway中C3 convertase的stabilization。 • Specific Fc receptors for IgA have been observed but are not well charaterized。
Formation of secretory IgA: • Dimer IgA binds to a poly-Ig receptor • Internalized by receptor-mediated endocytosis • Ploy-Ig receptor is enzymatically cleaved • Secretory component bound to the dimer IgA
IgE • 具有εheavy chain,κ或λlight chain,about 180 kDa,為所有Ig量最少的一種(約佔0.004%),為偵測allergic disorder(過敏性失調)之臨床標準指標值。 • 重鏈具有四個constant regions。 • 會與mast cells及basophils表面higt-affinity Fc receptor (FcεRI)接合,當有特殊抗原出現時,會刺激該細胞釋出inflammatory mediators。 • 某些細胞(such as eosinophils)表面受器FcεRII可與IgE接合(親和性低),對於parasitic worms感染之免疫性有重要關係。
Allergen cross-linkage of receptor-bound IgE on mast cell induces degranulation, causingrelease of substances that mediate allergic manifestations
IgD • 具有δheavy chain,κ或λlight chain,在血液及體液中出現濃度相當低。 • 目前研究發現在B細胞表面具有IgD,與IgM相連在一起;扮演B細胞表面的antigen receptor。 • 其與其他免疫球蛋白間之功能尚未明瞭。