Research Techniques Made Simple: Enzyme Immunoassay and ELISA

1. Research Techniques Made Simple:Enzyme Immunoassay and ELISA Stephanie D. Gan1and Kruti R. Patel2 1Department of Dermatology and 2 Program in Molecular and Translational Medicine, Department of Medicine, Boston University and Boston Medical Center

2. What is EIA/ELISA? • Enzyme immunosorbant (EIA) and enzyme-linked immunosorbant assay (ELISA) are commonly used biomedical techniques employed to detect and quantify specific antigens or antibodies in a given sample. • EIA and ELISA share similar basic principles. • Both are modified from the radioimmuno assay, in which the radioisotope is replaced with an enzyme.

3. What is EIA/ELISA? • EIA/ELISA is based on the immunologic concept of antigen binding to its specific antibody. • Allows detection of very small quantities of antigen, such as proteins, peptides, or hormones, or antibody in a sample. • Detection is qualitatively or quantitatively measured using an enzyme-labeled antigen or antibody to detect the sample antibody or antigen.

4. Primary antibody 2. Serum/Sample containing primary antibodies is added 1. Antigens coated onto the ELISA plate 96-well microtiter plate Secondary antibody E E E E E E E 4. Secondary antibody-conjugated with an enzyme is added 5. Excess secondary antibody is washed off the plate. 3. Non-antigen binding antibodies are washed off the plate Steps for performing ELISA E E E E E E Chromogen 7. Enzyme reacts with the substrate, producing color. color. Intensity of the color correlates with the level of antigen. 6. Substrate for the enzyme (Chromogen) is added

5. Types of ELISA • Indirect • Sandwich • Competitive • Multiple and portable

6. Indirect ELISA • Antibody or antigen is adhered to the microtiter wells. • Sample containing antibody/antigen is added • Secondary enzyme-conjugated antibody is added. • A substrate for the enzyme is introduced to quantify the primary antibody through color change. • Disadvantage: Method of antigen/antibody immobilization is non-specific.

7. Sandwich ELISA • Used to identify a sample antigen. • A known quantity of bound antibody is adhered to the mictotiter wells to capture antigen . • Antigen-containing sample is added and a specific antibody “sandwiches” the antigen. • Enzyme-linked secondary antibody is applied followed by a substrate to induce a color change. • Advantage: Eliminates the need to purify the antigen from a mixture of other antigens, simplifying the assay and increasing sensitivity and specificity.

8. Competitive ELISA • Central to this technique is the competitive binding between the sample antigen and antigen bound to the microtiter well with the antibody. • Primary unlabeled antibody is incubated with the sample antigen. • These antibody-antigen complexes are added to the well plates that are coated with the same antigen. • Any unbound antibody is washed off.

9. Competitive ELISA (cont.) • The more antigen in the sample, the more primary unlabeled antibody will be bound and thus less available to bind to the antigen in the well plate. • Secondary enzyme-linked antibody is added followed by substrate. • Absenceof color indicates a positive sample. • Advantage: High sensitivity to compositional differences in complex antigen mixtures, even when the specific detecting antibody is present in relatively small amounts.

10. Multiple and Portable ELISA • Uses a multicatcher device with 8 or 12 immunosorbant protruding pins on a central stick that is immersed in a sample. • Washings and incubation with antigens/antibodies and chromogen are performed by dipping the pins into pre-filled microwells with reagents. • Advantage: Ready-to-use kits, cheap, useful for large population screening, does not require skilled personnel or laboratory equipment. Ideal for low-resource settings.

11. Advantages/Limitations