Measurement in Science Bioassays and Immunoassays

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Measurement in Science Bioassays and Immunoassays Karim Meeran 23 October 2009

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Measurement in Science Bioassays and Immunoassays. Karim Meeran 23 October 2009. Assay. Method of measuring concentration of a hormone in body fluid (usually serum). Previously used “bioassay”. Bioassay. Administer extract of pituitary to animal and observe - PowerPoint PPT Presentation

Transcript of Measurement in Science Bioassays and Immunoassays

Page 1: Measurement in Science Bioassays and Immunoassays

Measurement in Science

Bioassays and Immunoassays

Karim Meeran

23 October 2009

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Assay

• Method of measuring concentration of a hormone in body fluid (usually serum).

• Previously used “bioassay”

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Bioassay

• Administer extract of pituitary to animal and observe

• (eg: LH would very slowly cause testicular enlargement).

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Bioassay

• Cells in vitro

• Grow

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Immunoassay

• Because antibody could bind to a particular protein, this could be used to measure the amount of a substance.

• Make antibody by giving protein to animal of different species

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• Assay for human adrenomedullin

• Give adrenomedullin to rabbits until they make antibodies (few months)

• Collect blood from the rabbits

• Use that blood to mop up antigen

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Principles of RIA

• Have known amount of radioactive adrenomedullin.

• Add unknown amount of unlabelled adrenomedullin

• Add measured amount of antibody

• Add a second antibody against the first

• Mix and spin

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Principles of RIA

• The second antibody may be a mouse anti rabbit antibody.

• This will be bound to a solid particle that will sink when centrifuged.

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Example

• Adrenomedullin paper

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Immunoassays

• Method of measuring concentration of a hormone in a body

• Two methods: - Competitive Assays

- Sandwich Assays

• Both work on the principle of enzyme specificity.

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Competitive assays

• For a given peptide (P) we are able to produce antibodies by administering the peptide to a different species.

E.g.: human peptide to rabbit.

• Let the rabbit make antibodies (Abr), after a couple months remove the blood and it will have Ab for this P

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Competitive assays

• Have Ab to P and we need to be able to accurately measure P. How do we do this:

• Make a Radioactive version of the peptide (Phot) and an Abm to the rabbit produce

• Abr into a mouse. But this Abm we also covalently attach to a particle of charcoal so it is heavier.

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Competitive Assays

A mixture of P and Phot

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Competitive Assays

A mixture of P and Phot

Addition of Abr which bind specifically to the peptides but cannot discriminate which ones are hot

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Competitive Assays

A mixture of P and Phot

Addition of Abr which bind specifically to the peptides but cannot discriminate which ones are hot

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Competitive Assays

A mixture of P and Phot

Addition of Abr which bind specifically to the peptides but cannot discriminate which ones are hot

Addition of excess Abm which binds to the Abr

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Competitive Assays

A mixture of P and Phot

Addition of Abr which bind specifically to the peptides but cannot discriminate which ones are hot

Addition of excess Abm which binds to the Abr

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Competitive Assays

A mixture of P and Phot

Addition of Abr which bind specifically to the peptides but cannot discriminate which ones are hot

Addition of excess Abm which binds to the Abr

Spin

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Competitive Assays

Following centrifugation, the supernatant and pellet need to be separated.

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Competitive Assays

Following centrifugation, the supernatant and pellet need to be separated.

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Competitive Assays

Following centrifugation, the supernatant and pellet need to be separated.

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Competitive Assays

Following centrifugation, the supernatant and pellet need to be separated.

Count BOUND radiation.

Count FREE radiation

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Competitive Assays

Following centrifugation, the supernatant and pellet need to be separated.

Count BOUND radiation.

50%

Count FREE radiation

50%

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Competitive Assays

Following centrifugation, the supernatant and pellet need to be separated.

Count BOUND radiation.

50%

Count FREE radiation

50%

Repeat for different concentrations of P

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Separating bound from free

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Bound to antibody + charcoal

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Competitive Assays

A mixture of P and Phot

Addition of Abr which bind specifically to the peptides but cannot discriminate which ones are hot

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Competitive Assays

A mixture of P and Phot

Addition of Abr which bind specifically to the peptides but cannot discriminate which ones are hot

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Competitive Assays

A mixture of P and Phot

Addition of Abr which bind specifically to the peptides but cannot discriminate which ones are hot

Addition of excess Abm which binds to the Abr

Spin

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Competitive Assays

Following centrifugation, the supernatant and pellet need to be separated.

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Competitive Assays

Following centrifugation, the supernatant and pellet need to be separated.

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Competitive Assays

Following centrifugation, the supernatant and pellet need to be separated.

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Competitive Assays

Following centrifugation, the supernatant and pellet need to be separated.

Count BOUND radiation.

Count FREE radiation

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Competitive Assays

Following centrifugation, the supernatant and pellet need to be separated.

Count BOUND radiation.

100%

Count FREE radiation

0%

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Competitive Assays

Following centrifugation, the supernatant and pellet need to be separated.

Count BOUND radiation.

100%

Count FREE radiation

0%

Repeat for different concentrations of P

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Competitive Assays

A mixture of P and Phot

Addition of Abr which bind specifically to the peptides but cannot discriminate which ones are hot

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Competitive Assays

A mixture of P and Phot

Addition of Abr which bind specifically to the peptides but cannot discriminate which ones are hot

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Competitive Assays

A mixture of P and Phot

Addition of Abr which bind specifically to the peptides but cannot discriminate which ones are hot

Addition of excess Abm which binds to the Abr

Spin

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Competitive Assays

Following centrifugation, the supernatant and pellet need to be separated.

Count BOUND radiation.

66%

Count FREE radiation

33%

Repeat for different concentrations of P

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Summary

Zero blue peptide gives 100% bound radiation.

Three blue peptide gives 66% bound radiation.

Twelve blue peptides gives 33% bound radiation.

This is the basis of how it works but for each assay we do using the antibodies we have we must run a series of these to obtain a reference curve.

Six blue peptide gives 50% bound radiation.

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What is serial dilution?

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Competitive Assays

Set up a series of tubes with known varying concentrations of P (achieved by serial dilution).

1 2 3 4

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Competitive Assays

Set up a series of tubes with known varying concentrations of P (achieved by serial dilution).

To all of these we add a set amount of Phot.1 2 3 4

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Competitive Assays• To each of these we add a set amount of Abr.

• This will bind randomly to the hot and cold peptides.

• Then add second antibody

1 2 3 4

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Competitive Assays• If the amount of Phot causes 1000 counts

• When we add Abm and centrifuge the mixtures we will be able to detect different amounts of radiation from the light and heavy regions of the mixtures.

1 23 4

667 counts

333 counts 500 counts 667 counts

500 counts 333 counts 0 counts

1000 counts

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Competitive Assays• If the amount of Phot causes 1000 counts

• When we add Abm and centrifuge the mixtures we will be able to detect different amounts of radiation from the light and heavy regions of the mixtures.

12 3

12 added

667 counts

None added

0 counts

1000 counts

B/F = infinite

6 added

500 counts

500 counts

B/F=1.0

3 added

333 counts

Heavy

Light

667 counts

B/F =2.0

333 counts

B/F=0.5

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Competitive assays

• This has allowed us to set up a graph which shows the counts against concentration of P.Counts

B/F ratio

2

1

0.5

0 3 6 12 Conc. Of P

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Competitive assays• We perform the same thing to a P of

unknown concentration, adding same amount of Phot and Abr and Abm as before.

• The count we get will allow us to extrapolate the value of P off the graph.

Counts

B/F ratio

2

1

0.5

0 3 6 12 Conc. Of P

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Immunoradiometric assay

• Two antibodies (monoclonal) to different epitopes of the protein.

• The first is bound to the tube.

• The second is radioactive.

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Sandwich Assays

• This is a different assay type but using the same principle of antibody specificity.

• Except we use MONOCLONAL antibodies.

• Therefore more expensive and takes longer.

• But more precise.

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Sandwich Assays• Here we are attaching one antibody (Abc)

to a surface.

• This Abc is specific to one part of the peptide (P) ie: the N-terminus

• We then expose the surface to P

• We wash way any remaining solution

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Sandwich Assays

• We then create an antibody (Abh) which is Radioactive

• This Abh is specific to the C-terminus of P.

• This is added to the surface.

• The excess solution is then washed away.

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Sandwich Assays

• As we did in the competetive assays we need to create a refrence chart for this assay. This is done by using different concentrations of P but set amount of Abc and Abh.

• We can then measure the concentration of P in our unknown solution.

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Sandwich Assays

• But in this type of assay we get a different sort of graph to extrapolate from.

Radioactive Count

Conc. Of P

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Practical planning

• Aim: to enable you to write up a practical that you have carried out

• The write up needs to be in the format of a paper for a journal.

• Abstract, aim, introduction, methods, results, discussion, references.

• You need to use refworks to reference it.