1. Affinity Chromatography

2. What is AC?
Affinity chromatography (AC) is a technique enabling purification of a biomolecule with respect to biological function or individual chemical structure.
AC is designed to purify a particular molecule from a mixed sample.

3. The resin
Matrix
Affinity Ligand

4. Step 1. Loading affinity column.

5. Step 2. Proteins sieve through matrix of affinity beads.

6. Step 3. Proteins interact with affinity ligand with some binding loosely and others tightly.

7. Step 4. Wash off proteins that do not bind.

8. Step 5. Wash off proteins that bind loosely.

9. Step 6. Elute proteins that bind tightly to ligand and collect purified protein of interest.

10. Affinity chromatography applied to recombinant proteins

11. Purity test
SDS-PAGE
Mass spectrometry
N-terminal sequencing, etc.

12. Downstream of protein purification
Biophysical characterization
Biochemical analysis of activities
Physiological relevance
Pathological mechanisms
etc.

13. Types of target molecular properties
Three groups of properties of the target molecule are used in affinity chromatography: 1. Specific binding properties based on biological activity like: - Enzyme active sites - Receptor binding sites - Antibody binding sites etc. These are used together with the natural ligand or an analogue of it. Sometimes the analogue has a broader specificity and can be used for group separations. 2. Naturally occurring prosthetic groups like: polysaccharides etc. Such properties normally allow group separations only. 3. Molecules equipped with an affinity tag like: - Glutathione-S-Transferase (GST) - Oligo histidine etc. This group of properties is used almost exclusively for recombinant fusion proteins.

15. In summary, Affinity chromatography is a method that will allow you to purify a particular molecule from a mixed sample so that further investigation of this molecule could be carried out.
Thank you for your attention.