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Enzym-gekoppelde immunosorbenttest
In 1971 ontwikkelden Peter Perlman en Eva Engvall een enzymgekoppelde immunosorbenttest (ELISA of EIA). ELISA verschilt van Western blot doordat de te…
Enzyme-linked immunosorbent assay or ELISA is a labeled immunoassay with wide applications in detecting and quantifying analytes like antibodies, peptides, glycoproteins, hormones, and viruses.
The detection antibodies that bind to the antigen or target molecule are conjugated with specific enzymes which, upon substrate addition, produce measurable signals.
Depending on the capture and detection methods, there are four major types of ELISA.
Direct ELISA uses an enzyme-conjugated primary antibody for detecting the sample antigen coated on the plate.
While for indirect ELISA, the attached antigen captures the sample primary antibody, to which the conjugated secondary antibody binds.
Sandwich ELISA involves two antibodies, one coated on the plate to capture the sample antigen, while the other enzyme-conjugated antibody binds to the specific antigen-epitope forming the sandwich.
In competitive ELISA, the antigen and the primary antibody are pre-incubated and added to the plate that is coated with the same antigen.
The higher the sample antigen concentration, the more antigen-antibody complexes are formed, leaving fewer free antibodies to bind to the competing antigen from the plate, therefore generating weaker signals.
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Q1: What is an enzyme-linked immunosorbent assay and what can it detect?
ELISA is a labeled immunoassay that detects and quantifies analytes including antibodies, peptides, glycoproteins, hormones, and viruses. Detection antibodies bind to target molecules and are conjugated with specific enzymes that produce measurable signals upon substrate addition. This versatile technique is widely used in diagnostics, pregnancy testing, food allergen detection, and cancer biomarker identification.
Q2: How does direct ELISA differ from indirect ELISA?
Direct ELISA uses a single enzyme-conjugated primary antibody to detect sample antigen coated on the plate. Indirect ELISA adds a secondary antibody for detection, making it more sensitive and flexible. The secondary antibody quantifies antigen-specific antibody presence by measuring color intensity from the conjugated enzyme-chromogen reaction.
Q3: When should sandwich ELISA be used instead of other ELISA types?
Sandwich ELISA is more specific and sensitive than direct and indirect formats, making it ideal for detecting large proteins with multiple epitopes. Two antibodies work together: one captures the sample antigen on the plate, while an enzyme-conjugated antibody binds to a specific epitope, forming a sandwich. The measured absorbance directly correlates to captured antigen amount.
Q4: What is the principle behind competitive ELISA?
In competitive ELISA, sample antigen and primary antibody are pre-incubated before adding to plate-coated antigen. Higher sample antigen concentration produces more antigen-antibody complexes, leaving fewer free antibodies to bind plate antigen, generating weaker signals. Signal intensity becomes inversely correlated to sample antigen concentration, allowing analyte quantification.
Q5: What enzymes and substrates are commonly used in ELISA?
Alkaline phosphatase and horseradish peroxidase are the most widely used enzymes in ELISA because appropriate substrates are readily available. The substrate is typically a chromogen, a colorless molecule converted into a colored end product by enzyme activity. Some ELISAs use fluorogens, nonfluorescent molecules converted to fluorescent forms, creating fluorescent enzyme immunoassays detectable by microscope or spectrophotometer.
Q6: Why is sandwich ELISA preferred for detecting small proteins?
Competitive ELISA is actually ideal for small protein detection because small molecules lack multiple epitopes needed for sandwich ELISA's two-antibody binding. Competitive ELISA allows crude samples to be used directly and offers highly flexible experimental setup. The assay's signal interference method enables accurate concentration determination for small analytes.
Q7: How does ELISA differ from Western blotting as a detection method?
ELISA assays are conducted in microtiter plates or in vivo, whereas Western blotting uses an absorbent membrane. Both techniques use antibodies conjugated to enzymes, but ELISA's microtiter plate format allows simultaneous processing of multiple samples. ELISA's enzyme-substrate reaction produces colored or fluorescent signals that can be visualized or quantified directly.