Focus on the adaptive immune system
Topics include antibody structure, function, interactions, and comparison between myoglobin and hemoglobin.
Two main types of immune systems in vertebrates: innate and adaptive.
Components include:
Skin and mucous membranes
Normal microflora
Phagocytic cells
Antimicrobial substances
Provides immediate defense against pathogens.
Composed of:
B cells: Produce antibodies and provide memory of past infections.
T cells: Present antigens and help eliminate pathogens.
Can adapt based on previous encounters with antigens.
B cells recognize antigens through immunoglobulin receptors on their surface.
Activation occurs when:
Antigens are internalized and presented with MHC class II.
T helper cells recognize the MHC-antigen complex and secrete cytokines.
B cells undergo clonal expansion, producing effector B cells (plasma cells) that secrete antibodies.
Five key roles:
Agglutination: Clumping of pathogens for easier phagocytosis.
Neutralization: Block binding of pathogens to target cells.
Opsonization: Enhancing phagocytosis through antibody coating.
Activation of Complement: Initiates inflammatory responses leading to cell lysis.
Binding of Effector Cells: Facilitating clearance of large antigens.
In primary response, immature B cells produce effector B cells (plasma cells).
Upon re-exposure to the same antigen, memory B cells enable a quicker and stronger secondary response by producing more antibodies.
Composed of four protein chains:
Two heavy chains
Two light chains
Bound together by di-sulfide bridges.
Each chain consists of a variable (V) region and a constant (C) region.
Binding sites formed by the combination of V regions specific to epitopes.
IgM: First response, large structure, effective in initiating the complement system.
IgG: Most abundant, crosses blood vessels and the placenta, binds antigens, and activates complement.
IgA: Present in secretions (saliva, tears), protects mucosal surfaces.
IgD: Found on B cell surfaces.
IgE: Involved in allergic responses, binds to mast cells.
Interactions occur via loops in the variable regions, which have unique shapes and charges that match specific antigens.
Includes complementarity determining regions (CDRs) that interact with antigens based on size and charge.
Shuffling of Nucleic Acid Sequences: Generates unique combinations of heavy and light chain regions.
Mutations in CDR Loops: Higher mutation rates that enhance antigen interaction properties without altering the overall structure of antibodies.