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  • Labeling of Proteins in vitro (S9110)

    Protocol

    1. Dissolve the vial of SNAP-Biotin (50 nmol) in 50 μl of fresh DMSO to yield a labeling stock solution of 1 mM SNAP-tag substrate. Mix by vortexing for 10 minutes until all the SNAP-tag substrate is dissolved. Dilute this 1 mM stock solution 1:4 in fresh DMSO to yield a 250 µM stock for labeling proteins in vitro.
    2. Set up the reactions, in order, as follows:
      Component Volume Final
      Concentration
      Phosphate Buffered Saline (PBS) 42 μl  1X
      50 mM DTT 1 μl 1 mM
      50 µM SNAP-tag
      Purified Protein
      5 μl 5 µM
      250 µM SNAP-tag
      Substrate
      2 μl 10 µM
      Total Volume 50 μl  
    3. Incubate in the dark for 30 minutes at 37°C.
    4. Run sample on an SDS-PAGE gel and detect using standard streptavidin-based detection reagents or store samples at -20°C or -80°C in the dark.

      Removal of Unreacted Substrate (optional)
      After the labeling reaction, the unreacted substrate can be separated from the labeled SNAP-tag fusion protein by gel filtration or dialysis. Please refer to the vendor’s instructions for the separation tools you are using.

      Notes for Labeling in vitro
      We recommend the routine addition of 1 mM DTT to all buffers used for handling, labeling and storage of the SNAP-tag. The stability of the SNAP-tag is improved in the presence of reducing agents; however it can also be labeled in their absence, if handling at temperatures above 4°C is minimized.

      SNAP-tag fusion proteins can be purified before labeling, but the labeling reaction also works in non-purified protein solutions (including cell lysates).

      Confirmation of Labeling by Western blot Analysis
      Labeled SNAP-tag fusion proteins can be easily analyzed on a SDS-PAGE gel/Western blot analysis because the covalently bound label will remain attached to the protein. The biotin label can be detected on an SDS-PAGE gel followed by Western blot using a Horseradish Peroxidase or Alkaline Phosphatase labeled avidin/streptavidin (e.g. streptavidin-HRP) and the corresponding detection method as described by the supplier of the enyzme conjugate.

      Troubleshooting for Labeling in vitro

      Solubility
      If solubility problems occur with your SNAP-tag fusion protein, we recommend testing a range of pH (pH 5.0–pH 10.0) and ionic strengths. The salt concentration may also need to be optimized for your particular fusion protein (50–250 mM).

      Loss of Protein Due to Aggregation or Sticking to Tube
      If stickiness of the fusion protein is a problem, we recommend adding Tween 20 at a final concentration of 0.05% to 0.1%. The SNAP-tag activity is not affected by this concentration of Tween 20. 

      Incomplete Labeling
      If exhaustive labeling of a protein sample is not achieved using the recommended conditions, try the following protocol modifications: Increase the incubation time to two hours total at 25°C or to 24 hours at 4°C; or halve the volume of protein solution labeled. Both approaches may be combined. If you still have poor labeling results, we recommend checking the activity of the SNAP-tag using SNAP-Vista Green.

      If the SNAP-tag fusion has been stored in the absence of DTT or other reducing agent, or has been stored at 4°C for a prolonged period, its activity may be compromised. Include 1 mM DTT in all solutions of the SNAP-tag fusion protein, and store the fusion protein at -20°C.

      Using less than the recommended amount of substrate stock solution can significantly slow down the reaction rate.

      Loss of Activity of Protein of Interest
      If your fusion protein is particularly sensitive to degradation or to loss of activity, you can try reducing the labeling time or decreasing the labeling temperature. If you label at 4°C we recommend overnight incubation.