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ANTIGENS Fe A. Bartolome, MD, FPASMAP Department of Microbiology Our Lady of Fatima University
IMMUNOGENS ,[object Object],[object Object],[object Object]
IMMUNOGENS ,[object Object],[object Object],[object Object],[object Object],[object Object]
ANTIGEN ,[object Object],[object Object],[object Object]
ANTIGEN ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
ANTIGEN ,[object Object],[object Object],[object Object],[object Object],[object Object]
ANTIGEN ,[object Object],[object Object],[object Object],[object Object]
HAPTEN ,[object Object],[object Object],[object Object],[object Object],[object Object]
EPITOPE ,[object Object],[object Object],[object Object],[object Object],[object Object]
Schematic representation of two antibodies interacting with linear and conformational epitopes.   a. Linear epitopes are  short and continuous . After denaturation the linear epitopes  may still be able to bind the antibody . b. Conformational epitopes are domains of proteins composed of specific regions of protein chains. After denaturation the discontinuous epitope  can no longer bind the antibody .
EPITOPE ,[object Object],[object Object],[object Object],[object Object]
EPITOPE B CELL EPITOPE Antigenic determinants are usually limited to those portions of the antigen that are accessible to antibodies shown in black for this iron-containing protein.
EPITOPE ,[object Object],[object Object],[object Object],[object Object]
ADJUVANT ,[object Object],[object Object],[object Object],[object Object],[object Object]
ADJUVANT ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
MAJOR HISTOCOMPATIBILITY COMPLEX
MHC  genes ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
MHC   glycoproteins ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Schematic representation depicting processing of antigens presented by class I MHC molecules.  (1) Intracellular proteins are proteolytically degraded within proteasomes    (2) yields antigenic peptides of 9 – 11 amino acids    (3) antigenic peptides are transported into the ER    (4) bind to newly synthesized class I MHC molecules    (5) Class I MHC-antigenic peptide complexes are exported through the Golgi and to the cell surface, for presentation of antigenic peptide to CD8 +  T cells. Cannon and Pate  Reproductive Biology and Endocrinology  2003 1:93   doi:10.1186/1477-7827-1-93
Calnexin (chaperone) assists in folding of MHC I proteins Calnexin released upon binding of  β 2m with MHC I proteins Degradation of cytosolic proteins into peptides by proteosome. Peptides transported into the ER via TAP (transporter for antigenic peptides) Tapasin – assists in peptide loading or transfer from TAP to MHC I protein) ERAP (endopasmic reticulum aminopeptidase) plays major role in trimming peptides to 8-11 aa to fit into MHC antigen binding pocket.
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Schematic representation depicting processing of antigens presented by class II MHC molecules.  (1) Extracellular and integral membrane proteins are internalized into endosomes via endocytosis    (2) Lysozomes fuse with endosomes. 3) Proteolytic degradation of endocytosed proteins resulting in the generation of antigenic peptides    (4) A specialized subcellualr organelle containing the class II MHC molecules, invariant chain, and DM fuses with the endolysozomal vesicle resulting in proteolytic degradation of invariant chain to CLIP. DM then catalyzes removal of CLIP, and the empty class II MHC molecules then bind antigenic peptides    (5) Class II MHC-antigenic peptide complexes are then exported to the cell surface, for presentation of antigenic peptide to CD4 +  T cells. Cannon and Pate  Reproductive Biology and Endocrinology  2003 1:93   doi:10.1186/1477-7827-1-93
Exogenous proteins degraded into peptides via enzyme GILT (gamma interferon inducible lysosomal thiol reductase) Invariant chain blocks binding of endogenous peptides Invariant chain degraded in endosomal compartment leaving CLIP in antigen binding compartment  Of MHC II protein Class II –associated invariant peptide HLA-DM & HLA-DO facilitate peptide loading on MHC II
 
MHC   glycoproteins ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Important Features of Some Human  MHC Gene Products Class I Class II Genetic loci (partial list) HLA-A, -B, and –C HLA-DP, -DQ, and  – DR Polypeptide composition MW 45,000 +   2 M (MW 12,000)    chain,    chain, and Ii chain Cell distribution All nucleated somatic cells Antigen-presenting cells, activated T cells Present peptide antigens to CD8+ T cells CD4+ T cells Size of peptide bound 8 – 11 residues 10 – 30 or more residues
Comparison of Class I and Class II MHC Proteins Feature Class I MHC Class II MHC Present antigen to CD4+ T cells No Yes  Present antigen to CD8+ T cells Yes No Found on surface of all nucleated cells Yes No Found on surface of professional APCs Yes Yes Encoded by genes in the HLA locus Yes Yes Expression of genes is codominant Yes Yes Multiple alleles at each gene locus Yes Yes Composed of 2 peptides encoded in HLA locus No Yes Composed of one peptide encoded in the HLA locus & a   2-microglobulin Yes No

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ANTIGENS Explained

  • 1. ANTIGENS Fe A. Bartolome, MD, FPASMAP Department of Microbiology Our Lady of Fatima University
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  • 10. Schematic representation of two antibodies interacting with linear and conformational epitopes. a. Linear epitopes are short and continuous . After denaturation the linear epitopes may still be able to bind the antibody . b. Conformational epitopes are domains of proteins composed of specific regions of protein chains. After denaturation the discontinuous epitope can no longer bind the antibody .
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  • 12. EPITOPE B CELL EPITOPE Antigenic determinants are usually limited to those portions of the antigen that are accessible to antibodies shown in black for this iron-containing protein.
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  • 19. Schematic representation depicting processing of antigens presented by class I MHC molecules. (1) Intracellular proteins are proteolytically degraded within proteasomes  (2) yields antigenic peptides of 9 – 11 amino acids  (3) antigenic peptides are transported into the ER  (4) bind to newly synthesized class I MHC molecules  (5) Class I MHC-antigenic peptide complexes are exported through the Golgi and to the cell surface, for presentation of antigenic peptide to CD8 + T cells. Cannon and Pate Reproductive Biology and Endocrinology 2003 1:93   doi:10.1186/1477-7827-1-93
  • 20. Calnexin (chaperone) assists in folding of MHC I proteins Calnexin released upon binding of β 2m with MHC I proteins Degradation of cytosolic proteins into peptides by proteosome. Peptides transported into the ER via TAP (transporter for antigenic peptides) Tapasin – assists in peptide loading or transfer from TAP to MHC I protein) ERAP (endopasmic reticulum aminopeptidase) plays major role in trimming peptides to 8-11 aa to fit into MHC antigen binding pocket.
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  • 22. Schematic representation depicting processing of antigens presented by class II MHC molecules. (1) Extracellular and integral membrane proteins are internalized into endosomes via endocytosis  (2) Lysozomes fuse with endosomes. 3) Proteolytic degradation of endocytosed proteins resulting in the generation of antigenic peptides  (4) A specialized subcellualr organelle containing the class II MHC molecules, invariant chain, and DM fuses with the endolysozomal vesicle resulting in proteolytic degradation of invariant chain to CLIP. DM then catalyzes removal of CLIP, and the empty class II MHC molecules then bind antigenic peptides  (5) Class II MHC-antigenic peptide complexes are then exported to the cell surface, for presentation of antigenic peptide to CD4 + T cells. Cannon and Pate Reproductive Biology and Endocrinology 2003 1:93   doi:10.1186/1477-7827-1-93
  • 23. Exogenous proteins degraded into peptides via enzyme GILT (gamma interferon inducible lysosomal thiol reductase) Invariant chain blocks binding of endogenous peptides Invariant chain degraded in endosomal compartment leaving CLIP in antigen binding compartment Of MHC II protein Class II –associated invariant peptide HLA-DM & HLA-DO facilitate peptide loading on MHC II
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  • 27. Important Features of Some Human MHC Gene Products Class I Class II Genetic loci (partial list) HLA-A, -B, and –C HLA-DP, -DQ, and – DR Polypeptide composition MW 45,000 +  2 M (MW 12,000)  chain,  chain, and Ii chain Cell distribution All nucleated somatic cells Antigen-presenting cells, activated T cells Present peptide antigens to CD8+ T cells CD4+ T cells Size of peptide bound 8 – 11 residues 10 – 30 or more residues
  • 28. Comparison of Class I and Class II MHC Proteins Feature Class I MHC Class II MHC Present antigen to CD4+ T cells No Yes Present antigen to CD8+ T cells Yes No Found on surface of all nucleated cells Yes No Found on surface of professional APCs Yes Yes Encoded by genes in the HLA locus Yes Yes Expression of genes is codominant Yes Yes Multiple alleles at each gene locus Yes Yes Composed of 2 peptides encoded in HLA locus No Yes Composed of one peptide encoded in the HLA locus & a  2-microglobulin Yes No