Презентация на тему Antigen-antibody reactions and selected tests

site of an antibody is located in the Fab

portion of the molecule and is constructed from the hypervariable regions of the heavy and light chains. Thus, the concept of antigen-antibody reactions is one of a key (i.e. the antigen) which fits into a lock (i.e.the antibody).

the reaction between a single antigenic determinant and a

single combining site on the antibody. It is the sum of the attractive and repulsive forces operating between the antigenic determinant and the combining site of the antibody as illustrated in Figure

of binding of an antigen with many antigenic determinants

and multivalent antibodies. Avidity is influenced by both the valence of the antibody and the valence of the antigen. Avidity is more than the sum of the individual affinities. This is illustrated in Figure.
To repeat, affinity refers to the strength of binding between a single antigenic determinant and an individual antibody combining site whereas avidity refers to the overall strength of binding between multivalent antigens and antibodies.

is shown as having three antigenic sites (epitopes). Two

are linear (solid box and shaded pentagon), and one is conformational dependent (shaded oval).
(i) to (iii) The orientation of the molecule on the well affects the presentation of the individual epitopes. This is true of passive and covalent binding to plastic.

Aggregation of the antigen can complicate presentation and also lead to leaching following binding with detecting antibody.
The antigen may be altered through treatment before attachment. In both (i) and (ii)the conformational epitope has been destroyed. Note also that the orientation of the molecules affects the presentation and spacing between individual epitopes.

Nondenatured protein can also alter its conformation by passive adsorption to plastic.

of an individual antibody combining site to react with

only
one antigenic determinant or the ability of a population of antibody molecules to react with only one antigen.
In general, there is a high degree of specificity in antigen-antibody reactions.

Antibodies can distinguish differences in:
The primary structure of an antigen
Isomeric forms of an antigen
Secondary and tertiary structure of an antigen

establishment of detection antibody titers (serodiagnosis);
 Diagnosis of diseases to

identify antigens of pathogens in the body;
Identification of cultures of bacteria and viruses isolated from humans and animals;
Determination of the composition and characteristics of human tissue: blood group, Rh factor, transplantation antigens;
Identification of the human body and in the environment of any substances having antigenicity (hormones, enzymes, toxins, drugs, drugs, etc.).
Assessment of immune status to determine the quantitative and functional characteristics of immune system cells and their products.
Identification of immunopathological conditions, allergies, transplant and anti-tumor responses.

APLICATION OF ANTIGEN-ANTIBODY REACTIONS 

an individual antibody combining site to react with more

than one antigenic determinant or the ability of a population of antibody molecules to react with more than one antigen. Figure illustrates how cross reactions can arise. Cross reactions arise because the cross reacting antigen shares an epitope in common with the immunizing antigen or because it has an epitope which is structurally similar to one on the immunizing antigen (multispecificity).

and precipitation of the bacteria under the influence of

antibodies in an environment with the electrolyte.

a thin film of the red blood cells glued

together (umbrella).

Passive Hemagglutination

antigen with antibody in the presence of electrolyte (NaCl)

complex Ag-Ab is formed as an insoluble precipitate.
PT is used for two purposes: detection of antigens with the help of known antibody or antibodies using known antigens.
With the help of PT falsification of fish and meat products is determined.

+
The test is carried

out by layering the antigen on the immune serum

carried out in agar gel plates or in Petri

dishes. Holes are cut out In the frozen gel at some distance from each other, and filled with the solutions of antigen and antisera. In the case of optimally selected ratio of antigens to antibodies, precipitation bands are formed in the gel between the wells. Since the reagents diffuse from the wells concentrically, the method allows several simultaneous reactions to be carried out by placing several wells with antigens around the antiserum well.

washed sheep RBCs)

2. Hemolysin (rabbit anti-sheep red-cell antibody)

3. Guinea

pig complement, free of antibodies to the agent of interest

4. Test serum

5. Antigen

illustrated in Figure. Antigen is mixed with the test

serum to be assayed for antibody and antigen/antibody complexes are allowed to form. A control tube in which no antigen is added is also prepared. If no antigen/antibody complexes are present in the tube, none of the complement will be fixed. However, if antigen/antibody complexes are present, they will fix complement and thereby reduce the amount of complement in the tube. After allowing complement fixation by any antigen/antibody complexes, a standard amount of red blood cells, which have been pre-coated with anti-erythrocyte antibodies is added. The amount of antibody-coated red blood cells is predetermined to be just enough to completely use up all the complement initially added, if it were still there.

consists of two stage:
First step (Complement fixation stage): a known

antigen and inactivated patient’s serum are incubated with a standardized, limited amount of complement. If the serum contains specific, complement activating antibody the complement will be activated or fixed by the antigen-antibody complex. However, if there is no antibody in the patient’s serum, there will be no formation of antigen-antibody complex, and therefore complement will not be fixed. But will remain free.

Second step (Indicator Stage): The second step detects whether complement has been utilized in the first step or not. This is done by adding the indicator system.
If the complement is fixed in the first step owing to the presence of antibody there will be no complement left to fix to the indicator system. There won’t be any lysis of RBCs.
However, if there is no antibody in the patient’s serum, there will be no antigen-antibody complex, and therefore, complement will be present free or unfixed in the mixture. This unfixed complement will now react with the antibody- coated sheep red blood cells to bring about their lysis.

Results and Interpretation
Thus, no lysis of sheep red blood cells (positive CFT) indicates the presence of antibody in the presence of antibody in the test serum, while lysis of sheep red blood cells (Negative CFT) indicates the absence of antibody in the serum.

test in which for the visualization of the formed

antigen-antibody complex enzyme labels (horseradish peroxidase or alkaline phosphatase) are used . These marker (indicator) enzymes are able to cleave the substrate and cause a color change.

the determination of antigens possessing more than one determinant.

In

the process of analysis, the antigen is "squeezed" between antibody molecules, which led to the name of the "sandwich" method. This name is now used practically in all literature as an official term.

Sandwich ELISA

конъюгат

диспенсер
автоматический
Автоматический гильотинный
резак
Вакуумный сушильный шкаф
для

упаковки тестов

контрольная зона)