DNA ligation

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==Notes==
==Notes==
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#If you are having trouble with your ligation, NEB offers [http://www.neb.com/nebecomm/products/faqproductM2200.asp FAQ] to help.
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#If you are having trouble with your ligation, NEB offers FAQ's [http://www.neb.com/nebecomm/products/faqproductM2200.asp] [http://www.neb.com/nebecomm/products/faqproductM0202.asp] to help.
#Prior to the ligation, some heat their DNA slightly (maybe ~37°C) to melt any sticky ends which may have annealed improperly at low temperatures.
#Prior to the ligation, some heat their DNA slightly (maybe ~37°C) to melt any sticky ends which may have annealed improperly at low temperatures.
#[[Tom Knight]] has read that ligase can inhibit transformation.  By heat-inactivating the ligase, this inhibition can be avoided.  However, according to the NEB FAQ, heat-inactivation of PEG (which is present in the ligation reaction) also inhibits transformation, therefore a spin-column purification is recommended prior to transformation if you are having problems.
#[[Tom Knight]] has read that ligase can inhibit transformation.  By heat-inactivating the ligase, this inhibition can be avoided.  However, according to the NEB FAQ, heat-inactivation of PEG (which is present in the ligation reaction) also inhibits transformation, therefore a spin-column purification is recommended prior to transformation if you are having problems.
#Treating PCR products with proteinase K prior to restriction digest dramatically improves the efficiency of subsequent ligation reactions.  See Crowe JS, Cooper HJ, Smith MA, Sims MJ, Parker D, Gewert D. Improved cloning efficiency of polymerase chain reaction (PCR) products after proteinase K digestion. ''Nucleic Acids Res''. 1991 Jan 11;19(1):184.
#Treating PCR products with proteinase K prior to restriction digest dramatically improves the efficiency of subsequent ligation reactions.  See Crowe JS, Cooper HJ, Smith MA, Sims MJ, Parker D, Gewert D. Improved cloning efficiency of polymerase chain reaction (PCR) products after proteinase K digestion. ''Nucleic Acids Res''. 1991 Jan 11;19(1):184.

Revision as of 16:43, 29 May 2006

Contents

General Information

DNA ligase is used to create a phosphodiester bond between the 5' phosphate and 3' hydroxyl groups of DNA. Most commonly, one needs to insert a DNA sequence of interest into a plasmid. Ideally, you can cut the DNA and vector with the same restriction enzyme. Then you can add both DNA sequences, the cut insert and vector sequence, and ligate them together to form a circular vector using DNA ligase. T4 DNA ligase is the most commonly used DNA ligase for molecular biology techniques.

General Procedure

The procedure for ligation depends upon whether the ligation is a blunt-end ligation or a ligation involving overlaps. Generally, you add the DNA you want to ligate, and then add a DNA ligase to ligate them together.

Specific Protocols

Endy:DNA ligation using T4 DNA ligase -- Using T4 DNA Ligase

Knight:DNA ligation using NEB Quick Ligation Kit -- We have a kit, so our procedure is different.

Knight:TOPO TA cloning -- For PCR products.

Silver: Ligation -- A protocol using the Roche Kit.

Notes

  1. If you are having trouble with your ligation, NEB offers FAQ's [1] [2] to help.
  2. Prior to the ligation, some heat their DNA slightly (maybe ~37°C) to melt any sticky ends which may have annealed improperly at low temperatures.
  3. Tom Knight has read that ligase can inhibit transformation. By heat-inactivating the ligase, this inhibition can be avoided. However, according to the NEB FAQ, heat-inactivation of PEG (which is present in the ligation reaction) also inhibits transformation, therefore a spin-column purification is recommended prior to transformation if you are having problems.
  4. Treating PCR products with proteinase K prior to restriction digest dramatically improves the efficiency of subsequent ligation reactions. See Crowe JS, Cooper HJ, Smith MA, Sims MJ, Parker D, Gewert D. Improved cloning efficiency of polymerase chain reaction (PCR) products after proteinase K digestion. Nucleic Acids Res. 1991 Jan 11;19(1):184.
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