Restriction Digest of Plasmid DNA
Restriction enzyme digestion takes advantage of naturally occurring enzymes that cleave DNA at specific sequences. There are hundreds of different restriction enzymes, allowing scientists to target a wide variety of recognition sequences. For a list of many commonly used restriction enzymes, visit NEB.
Last Upload: Oct. 11th, 2016
- Electrophoresis chamber
- Liquid DNA aliquot of your plasmid of interest (see below for recommend amounts)
- Appropriate restriction enzyme (see manufacturer's instructions for proper ammount)
- Approrpriate restriction digest buffer (see manufacturer's instructions)
- Gel loading dye
- Electrophoresis buffer
- Pipet tips
- Select restriction enzymes to digest your plasmid.
*Pro-Tip* To determine which restriction enzymes will cut your DNA sequence (and where they will cut), use a sequence analysis program such as Addgene's Sequence Analyzer.
- Determine an appropriate reaction buffer by reading the instructions for your enzyme.
*Pro-Tip* If you are conducting a double digest (digesting with two enzymes at the same time), you will need to determine the best buffer that works for both of your enzymes. Most companies will have a compatibility chart, such as the double digest finder tool from NEB.
In a 1.5mL tube combine the following:
- Restriction Enzyme(s)
- BSA (if recommended by manufacturer)
- dH2O up to total volume
*Pro-Tip* The amount of DNA that you cut depends on your application. Diagnostic digests typically involve ∼500 ng of DNA, while molecular cloning often requires 1-3 µg of DNA. The total reaction volume usually varies from 10-50 µL depending on application and is largely determined by the volume of DNA to be cut.*Pro-Tip* A typical restriction digestion reaction could look like this:
*Pro-Tip* The amount of restriction enzyme you use for a given digestion will depend on the amount of DNA you want to cut. By definition: one unit of enzyme will cut 1 µg of DNA in a 50 µL reaction in 1 hour. Using this ratio, you can calculate the minimal amount of enzyme for your reaction. However, keep in mind that restriction enzyme activity is determined under ideal conditions with very clean DNA, so using a little more enzyme is advisable. Reactions are often performed with 0.2-0.5 µL of enzyme because it is difficult to pipette less volume than this; 0.2-0.5 µL will likely be more enzyme than you will need, but that's okay because a little more enzyme is usually better.
- 1 µg DNA
- 1 µL of each Restriction Enzyme
- 3 µL 10x Buffer
- 3 µL 10x BSA (if recommended)
- x µL dH2O (to bring total volume to 30µL)
- Mix gently by pipetting.
- Incubate tube at appropriate temperature (usually 37 °C) for 1 hour. Always follow the manufacturer’s instructions.
- To visualize the results of your digest, conduct gel electrophoresis.
Tips and FAQ
- Restriction enzymes MUST be placed in an ice bucket immediately after removal from the -20 °C freezer because heat can cause the enzymes to denature and lose their function.
- If you are having difficulty finding an enzyme that cuts your vector's multiple cloning site (MCS), but does not cut your insert, you could try using two different enzymes that have compatible sticky ends. See NEB's compatible cohesive ends chart.
- If you cannot find compatible sticky ends, you will need to fill in the overhangs and conduct a blunt end ligation. Use T4 DNA Polymerase or Klenow DNA Polymerase I for 3′ overhang removal and 5′ overhang fill-in.
- If you are using blunt ends or a single enzyme to cut the vector, you will need to use a phosphatase to prevent re-circularization of the vector if you are cloning in an insert. CIP (calf alkaline phosphatase) or SAP (shrimp alkaline phosphatase) are commonly used. Follow the manufacturer’s instructions.
- If your enzyme did not cut, check to make sure that it isn't methylation sensitive. Plasmids grown in Dam or Dcm methylase positive strains will be resistant to cleavage at certain restriction sites. See NEB's table of methylation sensitive restriction sites.
- Sometimes enzymes cut sequences which are similar, but not identical, to their recognition sites. This is due to "Star Activity" and can happen for a variety of reasons, including high glycerol concentration. Learn more at NEB's website about star activity.
- If you are digesting a large number of plasmids with the same enzyme(s) (for instance, in a diagnostic digest), you can create a "Master Mix" consisting of all of the reaction components except for the DNA. Aliquot your DNA into individual tubes and then add the appropriate amount of Master Mix to each tube. This will save you time and ensure consistency across the reactions.