Gel electrophoresis is used to separate macromolecules like DNA, RNA and proteins. DNA fragments are separated according to their size. Proteins can be separated according to their size and their charge (different proteins have different charges).
How are DNA fragments separated using gel electrophoresis?
A solution ofmolecules is placed in a gel. Because each DNA molecule is negatively charged, it can be pulled through the gel by an electric field. Small DNA molecules move more quickly through the gel than larger DNA molecules.
The result is a series of ‘bands’, with each band containing DNA molecules of a particular size. The bands furthest from the start of the gel contain the smallest fragments of DNA. The bands closest to the start of the gel contain the largest DNA fragments.
When is gel electrophoresis used to separate DNA fragments?
can be used for a range of purposes, for example:
- To get a for purposes
- To get a DNA fingerprint for paternity testing
- To get a DNA fingerprint so that you can look for evolutionary relationships among organisms
- To check a PCR reaction.
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- To test for genes associated with a particular disease.
Find out more in the article,
When is gel electrophoresis used to separate proteins?
Thanks to TV shows like CSI, many people are familiar with the use of gelto separate macromolecules like DNA. However, gel electrophoresis can also be used to separate out proteins.
Different proteins have different sizes, mainly due to the number ofbuilding blocks in their structure. Chemical modifications attached to the also affect its size. Different proteins also have different charges. This can result from both the types of amino acid used to construct them, as well as the types of modifications attached to them.
Different types of electrophoresis gels are used to provide different types of information. The type of gel you choose therefore depends on the type of question you are asking.
Typically, gels made from polyacrylamide are used to separate proteins on the basis their different sizes. Usually, the proteins are first treated with heat and a chemical called SDS in order to unravel the protein. SDS is a detergent that gives all the proteins the same overall negative charge so that when an electric current is applied to the gel, separation is only due to the size of the protein. This technique is called SDS-PAGE (SDS-Polyacrylamide gel electrophoresis).
Small protein molecules move more quickly through the gel than larger proteins, resulting in a series of ‘bands’. Each band contains a protein of a particular size. These can be compared with standards of known sizes.
An SDS-PAGE gel has been used to separate proteins on the basis of size. The samples are the blood of various shark. The first lane contains markers of known sizes. Large proteins are at the top of the gel and small proteins are at the bottom.
This technique might be used for many purposes, including purifying a particular protein, for example to isolate anfor the food industry.
Charge and pH separation
Isoelectric focussing (IEF) and agarose gel electrophoresis are two ways that proteins can be separated by their different electrical charges. Unlike SDS-PAGE, the proteins are usually kept in their native (folded) state. The type of gel that is used, and the solution around the gel, are also different.
In agarose gel electrophoresis, proteins are loaded in the middle of the well. Those with a strong negative charge move fastest towards the positive side of the gel, whereas positively charged proteins move in the opposite direction.
This technique might be used to separate proteins that have the same molecular weight but different charges, or when size is not important (e.g. to look at changes in the presence of different protein during the development of a disease).
These days, charge (IEF) and size (SDS-PAGE) separation are often employed together in two-dimensional electrophoresis, where charge separation is first used, and then these separated proteins are separated on the basis on size.
This is a very effective method for identifying a particular protein from a tissue that may contain thousands of proteins and where there may only be small differences between control and treated samples (e.g. to look for a protein involved into insect predation in plants).