Immunoassays
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About This Presentation
immunoassay
Slide Content
Immunoassays
Prepared by:-
DhwaniKhandhar(19mph315)
M.PharmSem I
Department Of Pharmaceutical Analysis , NirmaUniversity
Prepared by:-
DhwaniKhandhar(19mph315)
M.PharmSem I
Department Of Pharmaceutical Analysis , NirmaUniversity
RADIOIMMUNOASSAY
RADIOIMMUNOASSAY
First developed by Yalow and Bersonin 1959& got Nobel prize in 1977
It has been improved dramatically in sensitivity and precision.
Very sensitive: can detect material present at concentrations of <0.001
micrograms/ml.
Numerous variations in the method have been introduced into the clinical
laboratory.
Two main RIA techniques
Competitive
Non-competitive heterogeneous formats
require washing steps to separate bound and free labels
First developed by Yalow and Bersonin 1959& got Nobel prize in 1977
It has been improved dramatically in sensitivity and precision.
Very sensitive: can detect material present at concentrations of <0.001
micrograms/ml.
Numerous variations in the method have been introduced into the clinical
laboratory.
Two main RIA techniques
Competitive
Non-competitive heterogeneous formats
require washing steps to separate bound and free labels
Radioimmunoassay (RIA)
Radioimmunoassay (RIA) –used radioisotopes as labels.
Allows the quantitative detection of a trace level of analytes
contributes to the advancement of basic research and clinical
medicine.
Generate standard curve with known amounts of unlabeled antigen
Measure unknown using standard curve.
RIA may be formatted in a solid phase procedure for easy separation
of bound and free labels.
Radioimmunoassay (RIA) –used radioisotopes as labels.
Allows the quantitative detection of a trace level of analytes
contributes to the advancement of basic research and clinical
medicine.
Generate standard curve with known amounts of unlabeled antigen
Measure unknown using standard curve.
RIA may be formatted in a solid phase procedure for easy separation
of bound and free labels.
RADIOIMMUNOASSAY
•The competitive assay follows:
THE LAW OF MASS ACTION
•The Scatchardplot of the ratio of bound to
free antibody to analyte concentration is
commonly used to evaluate antibody
performance.
•Kinetics of Antigen-Antibody Reaction section,
from the following equation:
B/F = Ka ([Ab]t − B)
Where, B = bound antigen or analyte
F = free antigen
•y-axis -B/F ratio that is proportional to free
[Ab] from [Ab]t − B, equal to free [Ag].
•Ka represents the slope of the plot.
Figure: Scatchardplot for
cyclosporine determination
The affinity constant Ka is 8.1 ×109 L/M
for the antibody specific to
cyclosporine.
•The competitive assay follows:
THE LAW OF MASS ACTION
•The Scatchardplot of the ratio of bound to
free antibody to analyte concentration is
commonly used to evaluate antibody
performance.
•Kinetics of Antigen-Antibody Reaction section,
from the following equation:
B/F = Ka ([Ab]t − B)
Where, B = bound antigen or analyte
F = free antigen
•y-axis -B/F ratio that is proportional to free
[Ab] from [Ab]t − B, equal to free [Ag].
•Ka represents the slope of the plot.
Figure: Scatchardplot for
cyclosporine determination
The affinity constant Ka is 8.1 ×109 L/M
for the antibody specific to
cyclosporine.
RADIOIMMUNOASSAY
Radioactive emissions, such as γ-rays of iodine-125 labels, can be measured
in terms of counts per minute (CPM) using a γ -scintillation counter.
The choice of label affects the assay protocol considerably.
Typical radioisotopes used as labels and their properties are shown below:
Radioactive emissions, such as γ-rays of iodine-125 labels, can be measured
in terms of counts per minute (CPM) using a γ -scintillation counter.
The choice of label affects the assay protocol considerably.
Typical radioisotopes used as labels and their properties are shown below:
CONVENTIONAL COMPETITIVE METHOD:
At first, known amounts of labeled antigen and antigen in
the specimen are mixed
Reacted competitively with a constant amount of antibody coated on a solid phase
After the immune reaction reaches its equilibrium, the mixture is washed.
It removes unreacted conjugates and antigens, and the immune complex trapped on the solid phase is separated.
RADIOIMMUNOASSAY -CONVENTIONAL
COMPETITIVE METHOD
At first, known amounts of labeled antigen and antigen in
the specimen are mixed
Reacted competitively with a constant amount of antibody coated on a solid phase
After the immune reaction reaches its equilibrium, the mixture is washed.
It removes unreacted conjugates and antigens, and the immune complex trapped on the solid phase is separated.
RADIOIMMUNOASSAY -CONVENTIONAL
COMPETITIVE METHOD
Assay principle of competitive radioimmunoassay
(RIA) using first antibody as solid phase.
(RIA) using first antibody as solid phase.
COMPETITIVE RADIOIMMUNOASSAY (RIA)
METHOD USING SECOND ANTIBODY
Thefirstantibodyspecifictoaparticularantigen(analyte)
reactscompetitivelywithboththeconjugateandthe
antigen.
Then,theimmunecomplexiscapturedbythesecond
antibodyspecifictothefirstantibody,onthesolidphase.
Whenthesecondantibodyiscoatedonafinesolidphase,
theimmunecomplexonthesecondreactioncanbe
separated.
Forantibodydetermination,labeledantibodyandantibody
inthespecimenreactcompetitivelywiththeantigen
(analyte)fixedonthesolidphase.
Thesteeperslopeofthestandardcurveprovidesmore
precisedata.
METHOD USING SECOND ANTIBODY
Thefirstantibodyspecifictoaparticularantigen(analyte)
reactscompetitivelywithboththeconjugateandthe
antigen.
Then,theimmunecomplexiscapturedbythesecond
antibodyspecifictothefirstantibody,onthesolidphase.
Whenthesecondantibodyiscoatedonafinesolidphase,
theimmunecomplexonthesecondreactioncanbe
separated.
Forantibodydetermination,labeledantibodyandantibody
inthespecimenreactcompetitivelywiththeantigen
(analyte)fixedonthesolidphase.
Thesteeperslopeofthestandardcurveprovidesmore
precisedata.
Assay principle of competitive radioimmunoassay (RIA) method
using second antibody for B/F (Bound/free) separation
using second antibody for B/F (Bound/free) separation
IMMUNORADIOMETRIC ASSAYS OR
SANDWICH ASSAYS(NON COMPETITIVE ASSAY)
Immunoradiometric assays orsandwich assays have alternative relationships
between analyte and antibody.
The classical competitive assay achieves an immunologic response with a
minimum amount of antibody; the sandwich assay uses a large amount of
antibodyon the solid phase.
Monoclonal antibody technology has made it possible to manufacture large
quantities of specific antibodies at moderate costs, thereby allowing the
sandwich assay to be exploited.
The sandwich assay, which uses excess antibody, is more sensitive than
the competitive assay
.
SANDWICH ASSAYS(NON COMPETITIVE ASSAY)
Immunoradiometric assays orsandwich assays have alternative relationships
between analyte and antibody.
The classical competitive assay achieves an immunologic response with a
minimum amount of antibody; the sandwich assay uses a large amount of
antibodyon the solid phase.
Monoclonal antibody technology has made it possible to manufacture large
quantities of specific antibodies at moderate costs, thereby allowing the
sandwich assay to be exploited.
The sandwich assay, which uses excess antibody, is more sensitive than
the competitive assay
.
IMMUNORADIOMETRIC ASSAYS OR
SANDWICH ASSAYS
The antibody on the solid phase first captures the antigen (analyte) in the specimen.
Following B/F separation, the conjugate reacts with the antigen (analyte) fixed on
the solid phase; the signal can then be counted after the elimination of free
conjugates through a washing step.
This assay requires antigens with more than two antigenic sites.
When two different antibodies (i.e., a solid-phase antibody specific to one antigenic
site and a conjugate antibody specific to another antigenic site) are used, the assay
protocol can be simplified by performing a one step sandwich.
Thus the solid phase can mix together with the antigen in the specimen and the
conjugate simultaneously.
SANDWICH ASSAYS
The antibody on the solid phase first captures the antigen (analyte) in the specimen.
Following B/F separation, the conjugate reacts with the antigen (analyte) fixed on
the solid phase; the signal can then be counted after the elimination of free
conjugates through a washing step.
This assay requires antigens with more than two antigenic sites.
When two different antibodies (i.e., a solid-phase antibody specific to one antigenic
site and a conjugate antibody specific to another antigenic site) are used, the assay
protocol can be simplified by performing a one step sandwich.
Thus the solid phase can mix together with the antigen in the specimen and the
conjugate simultaneously.
IMMUNORADIOMETRIC ASSAYS OR
SANDWICH ASSAYS
In this assay, the signal generated is proportional to the analyte concentration
present in the specimen, as in the two-step sandwich assay.
This assay method can be applied to antibody detection with an assay format
using antigen as the solid phase or labeled antigen.
For a two-step format, antigen as the solid phase or labeled antibody specific to
the target antibody can be used.
Using the sandwich format, assay sensitivity is highcompared to competitive
method
SANDWICH ASSAYS
In this assay, the signal generated is proportional to the analyte concentration
present in the specimen, as in the two-step sandwich assay.
This assay method can be applied to antibody detection with an assay format
using antigen as the solid phase or labeled antigen.
For a two-step format, antigen as the solid phase or labeled antibody specific to
the target antibody can be used.
Using the sandwich format, assay sensitivity is highcompared to competitive
method
Assay principle of sandwich radioimmunoassay (RIA) method
using solid phase, also referred to as immunoradiometric
assay. B/F, Bound/free.
using solid phase, also referred to as immunoradiometric
assay. B/F, Bound/free.
ENZYME IMMUNOASSAY
ENZYME IMMUNOASSAY
Quantitative immunoassays using enzymes as labels were developed as
alternatives to radioisotopes.
The most widely used are the
Enzyme-linked immunosorbent assay (ELISA)
Enzyme Immunoassay (EIA)
Enzyme-multiplied immunoassay technique (EMIT)
Essentially, heterogeneous EIAsare similar to RIAs, except that they use
enzymes as labels.
Improvements in EIAs have provided many innovative formats with different
degrees of speed, sensitivity, simplicity, and precision.
Quantitative immunoassays using enzymes as labels were developed as
alternatives to radioisotopes.
The most widely used are the
Enzyme-linked immunosorbent assay (ELISA)
Enzyme Immunoassay (EIA)
Enzyme-multiplied immunoassay technique (EMIT)
Essentially, heterogeneous EIAsare similar to RIAs, except that they use
enzymes as labels.
Improvements in EIAs have provided many innovative formats with different
degrees of speed, sensitivity, simplicity, and precision.
Enzyme immunoassay (EIA),
The enzyme immunoassay (EIA), uses enzymes as label.
Enzymes can amplify signals, depending on the turnover of enzyme catalytic
activity.
Efforts to improve substrates and to increase sensitivity have led to the
introduction of chromophore, fluorophore, and later chemiluminescent
compounds.
Depending on the substrate chosen, the assay method can be defined
Fluorescent enzyme immunoassay
Chemiluminescent enzyme immunoassay
The enzyme immunoassay (EIA), uses enzymes as label.
Enzymes can amplify signals, depending on the turnover of enzyme catalytic
activity.
Efforts to improve substrates and to increase sensitivity have led to the
introduction of chromophore, fluorophore, and later chemiluminescent
compounds.
Depending on the substrate chosen, the assay method can be defined
Fluorescent enzyme immunoassay
Chemiluminescent enzyme immunoassay
Advantages of Enzyme Immunoassay
1.Sensitive assays can be developed by the amplification effect of
enzymes.
2.Reagents are relatively cheap and can have a long shelf life.
3.Multiple simultaneous assays can be developed.
4.A wide variety of assay configurations can be developed.
5.Equipment can be inexpensive and is widely available.
6.No radiation hazards occur during labeling or disposal of wastes.
1.Sensitive assays can be developed by the amplification effect of
enzymes.
2.Reagents are relatively cheap and can have a long shelf life.
3.Multiple simultaneous assays can be developed.
4.A wide variety of assay configurations can be developed.
5.Equipment can be inexpensive and is widely available.
6.No radiation hazards occur during labeling or disposal of wastes.
Disadvantages of Enzyme Immunoassay
1.Measurement of enzyme activity can be more complex than measurement of
the activity of some types of radioisotopes.
2.Enzyme activity may be affected by plasma constituents.
3.Homogeneous assays at the present time have the sensitivity of 10
−9
M and are
not as sensitive as radio immunoassays.
4.Homogeneous EIAs for large protein molecules have been developed but
require complex immunochemical reagents
1.Measurement of enzyme activity can be more complex than measurement of
the activity of some types of radioisotopes.
2.Enzyme activity may be affected by plasma constituents.
3.Homogeneous assays at the present time have the sensitivity of 10
−9
M and are
not as sensitive as radio immunoassays.
4.Homogeneous EIAs for large protein molecules have been developed but
require complex immunochemical reagents
HETEROGENEOUS ENZYME
IMMUNOASSAYS
The assay principle of heterogeneous EIAs is similar to that of RIAs, except that
enzyme activity, not radioactivity, is measured .
EIAs require a secondary process to obtain signals through the catalytic reaction of
enzymes.
Microtiter plate wells, plastic beads, plastic tubes, magnetic particles, and latex
with filters, among others, can be used as the solid phase for the separation of
bound and free conjugates.
The use of small magnetic particles and latex allows shortening of the
immunoreaction time, thereby reducing the total assay time.
The development of substrates to be cleaved by enzymes was marked by the
introduction of colorimetric and fluorometric substrates, and later
chemiluminescent substrates, which increased the signal sensitivity.
The enzymes commonly used in various heterogeneous EIAs areperoxidase,
alkaline phosphatase, β-galactosidase, glucose oxidase, urease, and catalase.
IMMUNOASSAYS
The assay principle of heterogeneous EIAs is similar to that of RIAs, except that
enzyme activity, not radioactivity, is measured .
EIAs require a secondary process to obtain signals through the catalytic reaction of
enzymes.
Microtiter plate wells, plastic beads, plastic tubes, magnetic particles, and latex
with filters, among others, can be used as the solid phase for the separation of
bound and free conjugates.
The use of small magnetic particles and latex allows shortening of the
immunoreaction time, thereby reducing the total assay time.
The development of substrates to be cleaved by enzymes was marked by the
introduction of colorimetric and fluorometric substrates, and later
chemiluminescent substrates, which increased the signal sensitivity.
The enzymes commonly used in various heterogeneous EIAs areperoxidase,
alkaline phosphatase, β-galactosidase, glucose oxidase, urease, and catalase.
Characteristics of Typical Enzymes Used as Labels
for Enzyme Immunoassay
for Enzyme Immunoassay
Heterogeneous EIA
The solid phase with the attached reactants is mixed with
analyte, regardless of whether the assay is based on the
competitive or the non-competitive format.
Following the addition of conjugate and incubation, washing
steps are performed with a buffer solution containing a
detergent, one or two steps after the immuno reaction.
The solid phase, with the immunocomplex containing enzyme-
labeled antigen or antibody, is incubated at constant temperature with the enzyme–substrate solution.
The enzyme reaction is stopped (stopping is not needed in
rate assay), and the substrate reaction product is measured
with various detectors, depending on the substrate used.
The solid phase with the attached reactants is mixed with
analyte, regardless of whether the assay is based on the
competitive or the non-competitive format.
Following the addition of conjugate and incubation, washing
steps are performed with a buffer solution containing a
detergent, one or two steps after the immuno reaction.
The solid phase, with the immunocomplex containing enzyme-
labeled antigen or antibody, is incubated at constant temperature with the enzyme–substrate solution.
The enzyme reaction is stopped (stopping is not needed in
rate assay), and the substrate reaction product is measured
with various detectors, depending on the substrate used.
Assay principles of heterogeneous enzyme immunoassay (EIA)
using solid phase.
A, Competitive assay.
B and C, Noncompetitive sandwich assay.
using solid phase.
A, Competitive assay.
B and C, Noncompetitive sandwich assay.
Colorimetric Enzyme Immunoassay
In this assay, enzyme reaction is performed by using chromogenic
substrates to develop a color by prime catalytic reaction.
Example:
horseradish peroxidase, catalyzingABTS (diammonium salt of 2,2′-
azinodi[{ 3-ethyl-benzothiazoline-6-sulfonate}]) with H
2O
2to form a
green color
alkaline phosphatase specific to the p-nitrophenyl phosphate to form a
yellow color.
Both enzymes are the most commonly used types of colorimetric enzyme
immunoassays.
A spectrophotometer is used to measure the optical density of the
resulting chromogen.
Many instruments are available for the measurement of optical density in
tubes or microtiter plates, ranging from a fully automated system that
performs sample pipetting and data printout to simpler manual devices.
In this assay, enzyme reaction is performed by using chromogenic
substrates to develop a color by prime catalytic reaction.
Example:
horseradish peroxidase, catalyzingABTS (diammonium salt of 2,2′-
azinodi[{ 3-ethyl-benzothiazoline-6-sulfonate}]) with H
2O
2to form a
green color
alkaline phosphatase specific to the p-nitrophenyl phosphate to form a
yellow color.
Both enzymes are the most commonly used types of colorimetric enzyme
immunoassays.
A spectrophotometer is used to measure the optical density of the
resulting chromogen.
Many instruments are available for the measurement of optical density in
tubes or microtiter plates, ranging from a fully automated system that
performs sample pipetting and data printout to simpler manual devices.
Fluorescent Enzyme Immunoassay
Fluorescent EIAs are identical to other EIAs, except that they use fluorescent substrates
and a fluorophore is generated by an enzyme reaction.
Following excitation of the fluorophore at its optimal light excitation wavelength, light at
a characteristic wavelength is emitted.
Instruments such as a fluorometer require both a supplier of the excitation light source
and a photomultiplier tube as a detector of the emission fluorescence.
Substances that emit fluorescent light may be present in the specimen. These substances
may increase the background signal, which may interfere with the assay’s sensitivity.
Thus close attention should be paid to the selection of substrates for EIAs to avoid
interfering factors. Compared with colorimetric EIAs, fluorescent assays generate a signal
intensity that is at least one order of magnitude greater.
Fluorescent EIAs are identical to other EIAs, except that they use fluorescent substrates
and a fluorophore is generated by an enzyme reaction.
Following excitation of the fluorophore at its optimal light excitation wavelength, light at
a characteristic wavelength is emitted.
Instruments such as a fluorometer require both a supplier of the excitation light source
and a photomultiplier tube as a detector of the emission fluorescence.
Substances that emit fluorescent light may be present in the specimen. These substances
may increase the background signal, which may interfere with the assay’s sensitivity.
Thus close attention should be paid to the selection of substrates for EIAs to avoid
interfering factors. Compared with colorimetric EIAs, fluorescent assays generate a signal
intensity that is at least one order of magnitude greater.
Chemiluminescent Enzyme Immunoassay
Chemiluminescentenzyme immunoassays(CL-EIAs) use chemiluminescent
substrates that react with various enzymes employed as labels.
The chemiluminescent enzymatic reaction generates light, similar to
bioluminescence, which involves the use of natural substrates such as luciferin–
adenosine triphosphate.
These assays are effective tools in practical diagnosis.
The enzymatic oxidation reaction of luminol analogs has long been used for CL-EIA.
Use of peroxidase withH
2O
2is a common method that is interchangeable with an
alternative coupling enzyme producing H
2O
2,such as glucose oxidase or uricase.
Chemiluminescentenzyme immunoassays(CL-EIAs) use chemiluminescent
substrates that react with various enzymes employed as labels.
The chemiluminescent enzymatic reaction generates light, similar to
bioluminescence, which involves the use of natural substrates such as luciferin–
adenosine triphosphate.
These assays are effective tools in practical diagnosis.
The enzymatic oxidation reaction of luminol analogs has long been used for CL-EIA.
Use of peroxidase withH
2O
2is a common method that is interchangeable with an
alternative coupling enzyme producing H
2O
2,such as glucose oxidase or uricase.
HOMOGENEOUS ENZYME IMMUNOASSAYS
Conventional heterogeneous EIAs have equal sensitivity to RIAs in many
applications.
Various types of homogeneous EIAs are available.
In each of these assays, the Ag–Ab interaction modulates the activity of the
enzyme or enzyme label in the presence of the substrate. Modulation of the
enzyme activity reflects the degree of the immunochemical reaction.
Homogeneous EIAs can be classified as competitive and noncompetitive
binding assays.
Competitive assays usually consist of enzyme-labeled antigens. However, the
antigen (analyte) may be conjugated to the substrate or to a prosthetic group
of the enzyme in other assay formats.
In contrast, noncompetitive binding assays use a conjugate of antibody
labeled with enzyme.
Conventional heterogeneous EIAs have equal sensitivity to RIAs in many
applications.
Various types of homogeneous EIAs are available.
In each of these assays, the Ag–Ab interaction modulates the activity of the
enzyme or enzyme label in the presence of the substrate. Modulation of the
enzyme activity reflects the degree of the immunochemical reaction.
Homogeneous EIAs can be classified as competitive and noncompetitive
binding assays.
Competitive assays usually consist of enzyme-labeled antigens. However, the
antigen (analyte) may be conjugated to the substrate or to a prosthetic group
of the enzyme in other assay formats.
In contrast, noncompetitive binding assays use a conjugate of antibody
labeled with enzyme.
Classification and Characteristics of Typical
Homogeneous Enzyme Immunoassays
Homogeneous Enzyme Immunoassays
Enzyme-Multiplied Immunoassay
Technique (EMIT)
In EMIT, the conjugation of enzymes to haptens does not disrupt enzyme activity;
however, the binding of hapten-specific antibodies to haptensresults in inhibition of
enzyme activity.
Free haptensin the standard or sample relieve this inhibition by competing for
antibodies.
Thus in the presence of antibodies, enzyme activity is proportional to the
concentration of free haptens.
In the EMIT assay system, malate dehydrogenase and glucose -6-phosphate
dehydrogenase have been found to be most useful because they are less likely to be
affected by serum constituents.
These assays generally measure drugs at a concentration of milligrams per litre.
Technique (EMIT)
In EMIT, the conjugation of enzymes to haptens does not disrupt enzyme activity;
however, the binding of hapten-specific antibodies to haptensresults in inhibition of
enzyme activity.
Free haptensin the standard or sample relieve this inhibition by competing for
antibodies.
Thus in the presence of antibodies, enzyme activity is proportional to the
concentration of free haptens.
In the EMIT assay system, malate dehydrogenase and glucose -6-phosphate
dehydrogenase have been found to be most useful because they are less likely to be
affected by serum constituents.
These assays generally measure drugs at a concentration of milligrams per litre.
Enzyme-multiplied immunoassay technique (EMIT)
system diagram.
•The activity of an enzyme as a label is inhibited by the binding of antibody to
antigen (analyte) conjugated with enzyme.
•The analyte is usually a hapten. Glucose -6-phosphate dehydrogenase (G6PD) and
lysozyme are usually used as enzymes.
•In the assay, enzyme activity is proportionaltothe concentration of the analyte.
system diagram.
•The activity of an enzyme as a label is inhibited by the binding of antibody to
antigen (analyte) conjugated with enzyme.
•The analyte is usually a hapten. Glucose -6-phosphate dehydrogenase (G6PD) and
lysozyme are usually used as enzymes.
•In the assay, enzyme activity is proportionaltothe concentration of the analyte.
Substrate-LabeledFluorescent
Immunoassay
The substrate-labelled fluorescent immunoassay (SLFIA) uses a characteristic
fluorogenic substrate, umbelliferyl β-galactoside, attached to the antigen
(analyte) as a conjugate.
Umbelliferoneis the fluorescent product produced when the substrate is
cleaved with the enzyme β-galactosidase, which cannot cleave the substrate–
antigen complex when it is reacted with the specific antibody.
The free antigen (analyte) in the specimen solution competes with the
antigen conjugated with the substrate to form the immunocomplex.
The antigen concentration in the sample is proportional to the fluorescent
intensity of the cleaved fluorescent product.
SLFIA can be used to assay drugs and haptens , as well as protein ligands such
as IgG and IgM.
Immunoassay
The substrate-labelled fluorescent immunoassay (SLFIA) uses a characteristic
fluorogenic substrate, umbelliferyl β-galactoside, attached to the antigen
(analyte) as a conjugate.
Umbelliferoneis the fluorescent product produced when the substrate is
cleaved with the enzyme β-galactosidase, which cannot cleave the substrate–
antigen complex when it is reacted with the specific antibody.
The free antigen (analyte) in the specimen solution competes with the
antigen conjugated with the substrate to form the immunocomplex.
The antigen concentration in the sample is proportional to the fluorescent
intensity of the cleaved fluorescent product.
SLFIA can be used to assay drugs and haptens , as well as protein ligands such
as IgG and IgM.
Substrate-labelled fluorescent immunoassay
(SLFIA).
•Thesubstrateβ-galactosylumbeliferoneisconjugatedwiththeantigen(analyte)andformsa
nonfluorescentsubstrate.
•Thesubstratecanbecleavedbytheenzymeβ-galactosidasetoformafluorescentproduct.
•However,whenthesubstrate–antigenconjugateisallowedtoreactwithspecificantibodyto
theantigen,nocleavageofthesubstratecomplexwiththeβ-galactosidaseenzymeoccurs.
•Inthisassay,theconcentrationoftheantigen(analyte)isdirectlyproportionaltothe
fluorescentintensitymeasured.
(SLFIA).
•Thesubstrateβ-galactosylumbeliferoneisconjugatedwiththeantigen(analyte)andformsa
nonfluorescentsubstrate.
•Thesubstratecanbecleavedbytheenzymeβ-galactosidasetoformafluorescentproduct.
•However,whenthesubstrate–antigenconjugateisallowedtoreactwithspecificantibodyto
theantigen,nocleavageofthesubstratecomplexwiththeβ-galactosidaseenzymeoccurs.
•Inthisassay,theconcentrationoftheantigen(analyte)isdirectlyproportionaltothe
fluorescentintensitymeasured.
Apoenzyme Reactivation Immunoassay (ARIS)
ARIS is a homogeneous assay using the prosthetic group consisting of flavin
adenine dinucleotide (FAD)-conjugated antigen (analyte) and glucose oxidase
apoenzyme.
The antigen (analyte) and a constant amount of analyte–FAD conjugate compete for
a limited amount of specific antibody. At equilibrium, the level of free conjugate is
proportional to the amount of antigen (analyte) in thespecimen.
The apoenzyme combines with the free but not with the antibody-bound form of
conjugate to reactivate glucose oxidase activity in proportion to the amount of
free conjugate in the mixture.
Active enzyme is generated in the procedure, and an amplification mechanism is
built into this assay.
ARIS has been used to assay for theophylline and IgG, high-molecular-weight
proteins (e.g.,thyroidbinding globulin)as well as other haptenssuch as phenytoin
and hormones.
ARIS is a homogeneous assay using the prosthetic group consisting of flavin
adenine dinucleotide (FAD)-conjugated antigen (analyte) and glucose oxidase
apoenzyme.
The antigen (analyte) and a constant amount of analyte–FAD conjugate compete for
a limited amount of specific antibody. At equilibrium, the level of free conjugate is
proportional to the amount of antigen (analyte) in thespecimen.
The apoenzyme combines with the free but not with the antibody-bound form of
conjugate to reactivate glucose oxidase activity in proportion to the amount of
free conjugate in the mixture.
Active enzyme is generated in the procedure, and an amplification mechanism is
built into this assay.
ARIS has been used to assay for theophylline and IgG, high-molecular-weight
proteins (e.g.,thyroidbinding globulin)as well as other haptenssuch as phenytoin
and hormones.
Apoenzyme reactivation immunoassay
(ARIS)
Flavinadeninedinucleotide(FAD)
attachedtotheantigenisused.
Theapoenzymeisapoglucoseoxidase,
whichrequiresFADcofactorforactivity.
Intheassay,theconcentrationofantigen
(analyte)isproportionaltotheenzyme
activitygenerated.
(ARIS)
Flavinadeninedinucleotide(FAD)
attachedtotheantigenisused.
Theapoenzymeisapoglucoseoxidase,
whichrequiresFADcofactorforactivity.
Intheassay,theconcentrationofantigen
(analyte)isproportionaltotheenzyme
activitygenerated.
Enzyme Inhibitory Homogeneous
Immunoassay
Theenzymeα-amylasefromBacillussubtilis
ordextranasefromChaetomiumgracileis
conjugatedtothespecificantibodytothehigh-
molecular-weight antigen.
Thehighmolecular-weight antigencanbe
ferritinorα-fetoprotein.
Theα-amylaseenzymeisinactivewhenthe
enzymeantibodyconjugatereactswithspecific
antibody.
Theactiveenzymeformcanreactwiththe
starch-insolublesubstrate.Theantigen
concentrationisdirectlyproportionaltothe
enzymeactivityoftheassayreaction.
Immunoassay
Theenzymeα-amylasefromBacillussubtilis
ordextranasefromChaetomiumgracileis
conjugatedtothespecificantibodytothehigh-
molecular-weight antigen.
Thehighmolecular-weight antigencanbe
ferritinorα-fetoprotein.
Theα-amylaseenzymeisinactivewhenthe
enzymeantibodyconjugatereactswithspecific
antibody.
Theactiveenzymeformcanreactwiththe
starch-insolublesubstrate.Theantigen
concentrationisdirectlyproportionaltothe
enzymeactivityoftheassayreaction.
Cloned enzyme donor immunoassay (CEDIA).
•Enzyme acceptors associate with enzyme donors to form an active β-
galactosidase tetramer.
•The antibody inhibits the association of enzyme acceptor with enzyme
donor–antigenconjugate.
•Enzyme acceptors associate with enzyme donors to form an active β-
galactosidase tetramer.
•The antibody inhibits the association of enzyme acceptor with enzyme
donor–antigenconjugate.
Comparison of Radioimmunoassay, Heterogeneous Enzyme
Immunoassay, and Homogeneous Enzyme Immunoassay
Immunoassay, and Homogeneous Enzyme Immunoassay
REFERENCES:
McPherson RA, Pincus MR. Henry's Clinical Diagnosis and Management by
Laboratory Methods E-Book. Elsevier Health Sciences; 2017 Apr 5.p 862 -889.
McPherson RA, Pincus MR. Henry's Clinical Diagnosis and Management by
Laboratory Methods E-Book. Elsevier Health Sciences; 2017 Apr 5.p 862 -889.
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