0% found this document useful (0 votes)
59 views18 pages

Srtarting With The Name of Allah The Most Merciful and Mighty

Affinity chromatography is a technique that separates proteins based on a reversible interaction between a protein and a ligand coupled to a chromatographic matrix. It allows for purification of antibodies, antigens, hormones, or other proteins by taking advantage of their binding affinity for ligands. Compared to other techniques, affinity chromatography allows for purification that would otherwise be difficult or impossible and collects the target protein in a purified, concentrated form. The matrix provides support for ligand attachment, while the spacer arm improves binding by reducing steric hindrance between ligand and target.

Uploaded by

Yasir Khan
Copyright
© Attribution Non-Commercial (BY-NC)
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PPT, PDF, TXT or read online on Scribd
0% found this document useful (0 votes)
59 views18 pages

Srtarting With The Name of Allah The Most Merciful and Mighty

Affinity chromatography is a technique that separates proteins based on a reversible interaction between a protein and a ligand coupled to a chromatographic matrix. It allows for purification of antibodies, antigens, hormones, or other proteins by taking advantage of their binding affinity for ligands. Compared to other techniques, affinity chromatography allows for purification that would otherwise be difficult or impossible and collects the target protein in a purified, concentrated form. The matrix provides support for ligand attachment, while the spacer arm improves binding by reducing steric hindrance between ligand and target.

Uploaded by

Yasir Khan
Copyright
© Attribution Non-Commercial (BY-NC)
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PPT, PDF, TXT or read online on Scribd

SRTARTING WITH THE NAME OF ALLAH THE MOST MERCIFUL AND MIGHTY

AFFINITY CHROMATOGRAPHY

DEFINITION
Affinity chromatography separates proteins on the basis of a reversible interaction between a protein (or group of proteins) and a specific ligand coupled to a chromatographic matrix.

Affinity Chromatography is a relatively simple, yet quite effective molecular technique which isolates antibodies, antigens, hormones, or other proteins by taking advantage of their binding affinity for their respective ligands

Importance of affinity chromatography


Purification that would otherwise be timeconsuming, difficult or even impossible using other techniques can often be easily achieved with affinity chromatography Target protein(s) is collected in a purified, concentrated form.

Common terms in affinity chromatography


Matrix

Spacer arm

Ligand

MATRIX
For ligand attachment. Matrix should be chemically and physically inert.

SPACER ARM
Used to improve binding between ligand and target molecule by overcoming any effects of steric hindrance.

LIGANDS
Molecule that binds reversibly to a specific target molecule or group of target molecules.

Principle
The principle of affinity chromatography is as follows:
1) Inject a sample into an initially equilibrated affinity chromatography column. 2) Only the substances with affinity for the ligand are retained in the column. 3) Other substances with no affinity for the ligand are eluted from the column. 4) The substances retained in the column can be eluted from the column by changing pH or salt or organic solvent concentration of the eluent.

Affinity chromatography is widely used as a means of separation and purification with specific properties.

Affinity chromatography in practice


The first step towards a successful purification is to determine the availability of a suitable ligand that interacts reversibly with the target molecule or group of molecules.

Preparation of media and buffers


Storage solutions and preservatives should be washed away thoroughly before using any affinity medium.

Use high quality water and chemicals.


.

Solutions should be filtered through 0.45 m or 0.22 m filters.

Reuse of affinity media depends on the nature of the sample and should only be performed with identical samples to prevent cross contamination.

Avoid using magnetic stirrers as they may damage the matrix. Use mild rotation or end-over-end stirring.

You might also like