Antibodies are produced by plasma cells. Fig. 6.1 shows antigens bound to antigen-binding sites of an antibody molecule. [Figure 6.1] It is estimated that the immune system of each person can make enough antibodies to bind to over 10¹² different antigens. When plasma cells make antibody molecules they combine the polypeptides produced by the expression of genes for heavy chains and the genes for light chains. Research has shown that producing this very large number of antibodies is only possible by modifying the primary transcripts of the genes that code for heavy chains and the genes that code for light chains.
- (a)(i)Explain how the structure of an antigen-binding site makes it specific to a particular antigen, as shown in Fig. 6.1.[2]
- (a)(ii)State the function of the hinge region of the antibody shown in Fig. 6.1.[1]
- (a)(iii)Antibodies can bind to membrane receptors on cells of the immune system, such as macrophages. Suggest an advantage of antibodies binding to receptors on macrophages.[1]
- (b)Suggest how this modification of the primary transcripts occurs in plasma cells.[2]
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Mark scheme
Marking points from the official mark scheme (May/June 2024). The mark or mark type is shown in brackets.
- [2] any two from:
- [2] 1 (antigen-binding site / variable region) has a shape that is complementary to antigen; A tertiary / quaternary, structure
- [2] 2 (antigen-binding site / variable region has) specific, sequence(s) of amino acids / primary structure(s);
- [2] 3 idea that different amino acids have different, R-groups / side chains, so give different, tertiary structures / shapes (for binding to antigens);
- [2] 4 AVP; e.g. correct ref. to epitope(s)
- [1] idea that allows flexibility for binding (to antigens) ; A at different angles for flexibility / allows variable region(s) to move
- [1] any one from:
- [1] idea that easier for macrophage to engulf, antibodies that have bound antigens / antibody-antigen complexes ;
- [1] facilitates / AW, destruction of pathogens 'marked' by antibodies ; A ref. to opsonisation I stimulates phagocytosis of the pathogen, unqualified
- [2] any two from:
- [2] 1 removal of introns (from primary transcript);
- [2] 2 (after removal of introns) exons, are joined together, in different, sequences / combination(s) ; A alternative splicing
- [2] 3 not all the exons are used (in making the polypeptides) ; I capping and poly-A tails
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