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Affinity Chromatography

This is a brief overview of the mechanism, procedure, and applications of affinity chromatography.

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SYED MUHAMMAD KHAN (BS HONS. ZOOLOGY)
1
Affinity Chromatography
Chromatography is a powerful analytical technique used to separate a mixture into its
parts. There are many different types of chromatography — but they all rely on a process
using the different properties that exist between the target molecule (the molecule of
interest) and its matrix, which together make-up the sample.
Figure: Types of chromatography & the main forces in action.
Liquid chromatography uses a liquid to carry the sample across a stationary phase where
the separation takes place, and is one of the main techniques used in biological sciences
due to its ability to separate samples at relatively low temperatures (as opposed to gas
chromatography which operates at high temperatures).
Affinity Chromatography
One of the lesser-known liquid chromatography techniques is affinity chromatography —
a technique important in pharmaceutical science and biotechnology. But what is affinity
chromatography?
SYED MUHAMMAD KHAN (BS HONS. ZOOLOGY)
2
Affinity chromatography is a separation method based on a specific binding interaction
between an immobilized ligand and its binding partner. Examples include
antibody/antigen, enzyme/substrate, and enzyme/inhibitor interactions. The degree of
purification can be quite high depending on the specificity of the interaction and,
consequently, it is generally the first step, if not the only step, in a purification strategy.
Figure: Principle of Affinity Chromatography.
Chromatography relies on stationary and mobile phases. In affinity chromatography the
stationary phase is critical — and is made up of a solid support (a chemically and
biologically inert medium) and a binding agent, the affinity ligand, (that selectively binds
to the target molecule) in a column.
Components of Affinity Chromatography
Matrix: The matrix is an inert support to which a ligand can be directly or indirectly
coupled. For the matrix to be effective it must have certain characters:
 Matrix should be chemically and physically inert.
 It must be insoluble in solvents and buffers employed in the process.
SYED MUHAMMAD KHAN (BS HONS. ZOOLOGY)
3
 It must be chemically and mechanically stable.
 It must be easily coupled to a ligand or spacer arm onto which the ligand can be
attached.
 It must exhibit good flow properties and have a relatively large surface area for
attachment.
 The most useful matrix materials are agarose and polyacrylamide.
Spacer arm: It is used to improve binding between ligand and target molecule by
overcoming any effects of steric hindrance.
Ligand: It refers to the molecule that binds reversibly to a specific target molecule. The
ligand can be selected only after the nature of the macromolecule to be isolated is known.
When a hormone receptor protein is to be purified by affinity chromatography, the
hormone itself is an ideal candidate for the ligand. For antibody isolation, an antigen may
be used as a ligand. If an enzyme is to be purified, a substrate analog, inhibitor, cofactor,
or effector may be used as the immobilized ligand.
Basic Steps of Affinity Chromatography
Affinity chromatography can be described in basic steps:
 The column and stationary phase are flushed with a buffer solution to prepare the
ligands for binding.
 The sample is introduced under conditions that favor the binding of the target
molecules to the affinity ligands. The target molecules bind to the ligands and the
unbound molecules are washed away.
 By changing the elution conditions or using another ligand, the target molecules
are freed from the ligands and elute from the column giving a purified protein.
The events depicted in the diagram above can be summarized into the following three
major steps:
SYED MUHAMMAD KHAN (BS HONS. ZOOLOGY)
4
1. Preparation of Column: The column is loaded with solid support such as
sepharose, agarose, cellulose, etc. Ligand is selected according to the desired
isolate. The spacer arm is attached between the ligand and solid support.
2. Loading of Sample: Solution containing a mixture of substances is poured into the
elution column and allowed to run at a controlled rate.
3. Elution of Ligand-Molecule Complex: The target substance is recovered by
changing conditions to favor elution of the bound molecules.
Figure: Mechanism of Affinity Chromatography
Mechanism of Affinity Binding
A commonly used metaphor to illustrate affinity binding is the lock and key analogy. A
unique structure present on the surface of a protein is the key that will only bind to the
corresponding lock, a specific ligand on a chromatographic support.
Affinity-tagged Purification
In two-step affinity-tagged protein purification, a protein is first purified by affinity
chromatography, then desalted. In some medium pressure chromatography systems,
SYED MUHAMMAD KHAN (BS HONS. ZOOLOGY)
5
such as the NGC medium pressure chromatography systems, these two steps can be
automated. In the first step, a recombinant protein mixture is passed over a
chromatography support containing a ligand that selectively binds proteins that contain
an affinity-tag sequence. Contaminants are washed away, and the bound protein is then
eluted in pure form.
Affinity tags have different advantages. In immobilized metal affinity chromatography
(IMAC), His binds with good selectivity to Ni2+ or other transition metals immobilized to
the ligand; the tagged protein can be selectively eluted with imidazole. Tagged proteins
bind to glutathione as the ligand, and are eluted with solutions of glutathione.
During the second step of desalting, affinity-purified samples can simultaneously undergo
buffer exchange to remove salts in preparation for downstream applications. Several
desalting techniques, including size exclusion chromatography, dialysis, and
ultrafiltration, also allow buffer exchange. Desalting often includes the removal not only
of salt, but also of other foreign substances, such as detergents, nucleotides, and lipids.
Types of Affinity Chromatography
Affinity chromatography can be broadly divided into two method types:
1. The first method uses a naturally occurring structure or sequence of amino acids
on the protein as the binding site. Examples include the affinity of Affi-Gel Blue
support binding for albumin’s bilirubin-binding site and the binding of protein A in
the Affi-Gel and Affi-Prep protein A supports to the Fc region of IgG. An important
consideration for antibody purification is to determine the affinity of your target
antibody for protein A/G chromatography media, which varies widely.
2. The second method involves binding to a special amino acid sequence engineered
into the protein of interest, commonly referred to as a "tag". Several different tags
SYED MUHAMMAD KHAN (BS HONS. ZOOLOGY)
6
are available. Two of the most commonly used protein tags are the polyhistidine
tag, which binds to certain metal-containing complexes such as those in Profinity
IMAC resins, and the glutathione s-transferase (GST) sequence, which binds to
glutathione, found in Bio-Scale Mini Profinity GST media. Theoretically, any protein
can be purified using the tagging method; however, many factors must be
considered to design a process to purify tagged recombinant proteins.
General Considerations for Affinity Purification
The binding and elution conditions in affinity chromatography can vary greatly, however,
there are some general guidelines. Because most binding interactions are based on those
formed in nature, the conditions similar to those present in most cellular organisms are
usually the best binding conditions. Therefore PBS (phosphate-buffered saline) is often
the buffer of choice. Conversely, conditions not normally found in vivo may alter the
protein structure enough to cause the protein to dissociate from the ligand. In situations
where there is no recommended elution condition, a low pH (>4) will often elute bound
protein with an inherent risk of denaturation.
Applications of Affinity Chromatography
Affinity chromatography is one of the most useful methods for the separation and
purification of specific products. It is essentially a sample purification technique, used
primarily for biological molecules such as proteins.
Affinity chromatography offers high selectivity, resolution, and capacity in most protein
purification schemes. It has the advantage of utilizing a protein's biological structure or
function for purification. As a result, purifications that would otherwise be time-consuming
and complicated can often be easily achieved with affinity chromatography.
Its major application includes:
 Separation of a mixture of compounds

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Affinity Chromatography

  • 1. SYED MUHAMMAD KHAN (BS HONS. ZOOLOGY) 1 Affinity Chromatography Chromatography is a powerful analytical technique used to separate a mixture into its parts. There are many different types of chromatography — but they all rely on a process using the different properties that exist between the target molecule (the molecule of interest) and its matrix, which together make-up the sample. Figure: Types of chromatography & the main forces in action. Liquid chromatography uses a liquid to carry the sample across a stationary phase where the separation takes place, and is one of the main techniques used in biological sciences due to its ability to separate samples at relatively low temperatures (as opposed to gas chromatography which operates at high temperatures). Affinity Chromatography One of the lesser-known liquid chromatography techniques is affinity chromatography — a technique important in pharmaceutical science and biotechnology. But what is affinity chromatography?
  • 2. SYED MUHAMMAD KHAN (BS HONS. ZOOLOGY) 2 Affinity chromatography is a separation method based on a specific binding interaction between an immobilized ligand and its binding partner. Examples include antibody/antigen, enzyme/substrate, and enzyme/inhibitor interactions. The degree of purification can be quite high depending on the specificity of the interaction and, consequently, it is generally the first step, if not the only step, in a purification strategy. Figure: Principle of Affinity Chromatography. Chromatography relies on stationary and mobile phases. In affinity chromatography the stationary phase is critical — and is made up of a solid support (a chemically and biologically inert medium) and a binding agent, the affinity ligand, (that selectively binds to the target molecule) in a column. Components of Affinity Chromatography Matrix: The matrix is an inert support to which a ligand can be directly or indirectly coupled. For the matrix to be effective it must have certain characters:  Matrix should be chemically and physically inert.  It must be insoluble in solvents and buffers employed in the process.
  • 3. SYED MUHAMMAD KHAN (BS HONS. ZOOLOGY) 3  It must be chemically and mechanically stable.  It must be easily coupled to a ligand or spacer arm onto which the ligand can be attached.  It must exhibit good flow properties and have a relatively large surface area for attachment.  The most useful matrix materials are agarose and polyacrylamide. Spacer arm: It is used to improve binding between ligand and target molecule by overcoming any effects of steric hindrance. Ligand: It refers to the molecule that binds reversibly to a specific target molecule. The ligand can be selected only after the nature of the macromolecule to be isolated is known. When a hormone receptor protein is to be purified by affinity chromatography, the hormone itself is an ideal candidate for the ligand. For antibody isolation, an antigen may be used as a ligand. If an enzyme is to be purified, a substrate analog, inhibitor, cofactor, or effector may be used as the immobilized ligand. Basic Steps of Affinity Chromatography Affinity chromatography can be described in basic steps:  The column and stationary phase are flushed with a buffer solution to prepare the ligands for binding.  The sample is introduced under conditions that favor the binding of the target molecules to the affinity ligands. The target molecules bind to the ligands and the unbound molecules are washed away.  By changing the elution conditions or using another ligand, the target molecules are freed from the ligands and elute from the column giving a purified protein. The events depicted in the diagram above can be summarized into the following three major steps:
  • 4. SYED MUHAMMAD KHAN (BS HONS. ZOOLOGY) 4 1. Preparation of Column: The column is loaded with solid support such as sepharose, agarose, cellulose, etc. Ligand is selected according to the desired isolate. The spacer arm is attached between the ligand and solid support. 2. Loading of Sample: Solution containing a mixture of substances is poured into the elution column and allowed to run at a controlled rate. 3. Elution of Ligand-Molecule Complex: The target substance is recovered by changing conditions to favor elution of the bound molecules. Figure: Mechanism of Affinity Chromatography Mechanism of Affinity Binding A commonly used metaphor to illustrate affinity binding is the lock and key analogy. A unique structure present on the surface of a protein is the key that will only bind to the corresponding lock, a specific ligand on a chromatographic support. Affinity-tagged Purification In two-step affinity-tagged protein purification, a protein is first purified by affinity chromatography, then desalted. In some medium pressure chromatography systems,
  • 5. SYED MUHAMMAD KHAN (BS HONS. ZOOLOGY) 5 such as the NGC medium pressure chromatography systems, these two steps can be automated. In the first step, a recombinant protein mixture is passed over a chromatography support containing a ligand that selectively binds proteins that contain an affinity-tag sequence. Contaminants are washed away, and the bound protein is then eluted in pure form. Affinity tags have different advantages. In immobilized metal affinity chromatography (IMAC), His binds with good selectivity to Ni2+ or other transition metals immobilized to the ligand; the tagged protein can be selectively eluted with imidazole. Tagged proteins bind to glutathione as the ligand, and are eluted with solutions of glutathione. During the second step of desalting, affinity-purified samples can simultaneously undergo buffer exchange to remove salts in preparation for downstream applications. Several desalting techniques, including size exclusion chromatography, dialysis, and ultrafiltration, also allow buffer exchange. Desalting often includes the removal not only of salt, but also of other foreign substances, such as detergents, nucleotides, and lipids. Types of Affinity Chromatography Affinity chromatography can be broadly divided into two method types: 1. The first method uses a naturally occurring structure or sequence of amino acids on the protein as the binding site. Examples include the affinity of Affi-Gel Blue support binding for albumin’s bilirubin-binding site and the binding of protein A in the Affi-Gel and Affi-Prep protein A supports to the Fc region of IgG. An important consideration for antibody purification is to determine the affinity of your target antibody for protein A/G chromatography media, which varies widely. 2. The second method involves binding to a special amino acid sequence engineered into the protein of interest, commonly referred to as a "tag". Several different tags
  • 6. SYED MUHAMMAD KHAN (BS HONS. ZOOLOGY) 6 are available. Two of the most commonly used protein tags are the polyhistidine tag, which binds to certain metal-containing complexes such as those in Profinity IMAC resins, and the glutathione s-transferase (GST) sequence, which binds to glutathione, found in Bio-Scale Mini Profinity GST media. Theoretically, any protein can be purified using the tagging method; however, many factors must be considered to design a process to purify tagged recombinant proteins. General Considerations for Affinity Purification The binding and elution conditions in affinity chromatography can vary greatly, however, there are some general guidelines. Because most binding interactions are based on those formed in nature, the conditions similar to those present in most cellular organisms are usually the best binding conditions. Therefore PBS (phosphate-buffered saline) is often the buffer of choice. Conversely, conditions not normally found in vivo may alter the protein structure enough to cause the protein to dissociate from the ligand. In situations where there is no recommended elution condition, a low pH (>4) will often elute bound protein with an inherent risk of denaturation. Applications of Affinity Chromatography Affinity chromatography is one of the most useful methods for the separation and purification of specific products. It is essentially a sample purification technique, used primarily for biological molecules such as proteins. Affinity chromatography offers high selectivity, resolution, and capacity in most protein purification schemes. It has the advantage of utilizing a protein's biological structure or function for purification. As a result, purifications that would otherwise be time-consuming and complicated can often be easily achieved with affinity chromatography. Its major application includes:  Separation of a mixture of compounds
  • 7. SYED MUHAMMAD KHAN (BS HONS. ZOOLOGY) 7  Removal of impurities or in purification process  In enzyme assays  Detection of substrates  Investigation of binding sites of enzymes  In in vitro antigen-antibody reactions  Detection of Single Nucleotide polymorphisms and mutations in nucleic acids Advantages of Affinity Chromatography  High specificity  Target molecules can be obtained in a highly pure state  Single-step purification  The matrix can be reused rapidly  The matrix is a solid, can be easily washed and dried  Give purified product with high yield  Affinity chromatography can also be used to remove specific contaminants, such as proteases Limitations of Affinity Chromatography  Time-consuming method  More amounts of solvents are required which may be expensive  Intense labor  Non-specific adsorption cannot be eliminated, it can only be minimized  Limited availability and high cost of immobilized ligands  Proteins get denatured if required pH is not adjusted