Once the building block has been converted into a BC-substrate it can be used to label CLIP-tag fusion proteins. These can be labeled in cell lysates or as purified protein.
For labeling, we recommend using a 1.5 fold excess of substrate to CLIP-tag fusion protein and incubation for 1 hour at room temperature. Typical concentrations are 30 µM substrate and 20 µM CLIP-tag fusion protein. The labeling incubation can be followed by a separation step such as dialysis or spin column separation to remove unreacted substrate, if desired.
Unlabeled protein samples should be stored at -20°C, or at -80°C for long-term storage. Many proteins benefit from the addition of glycerol for frozen storage, typically 20% v/v. Handling at temperatures above 0°C should be minimized by thawing the unlabeled protein samples shortly before use, and keeping them on ice until just before the labeling reaction.
We recommend the routine addition of 1 mM DTT to all buffers used for handling, labeling and storage of CLIP-tag fusion proteins. The stability of the CLIP-tag is improved in the presence of reducing agents; however it can also be labeled in their absence.
If a particular fusion protein requires buffers without reducing agents, minimize all handling steps of the protein above 4°C prior to the labeling reaction.
The CLIP-tag labeling reaction works well between pH 5.0 and pH 10.0 The salt concentration may need to be optimized for your particular fusion protein, although the CLIP-tag labeling reaction has been shown to work at a broad range of ionic strengths (NaCl concentrations between 15 mM and 1 M). If the buffer conditions used for labeling lead to insolubility of your protein, we recommend testing a range of pH and ionic strengths. For a range of fusion proteins we have found ionic strengths for monovalent salts (e.g. sodium chloride) from 50 mM to 250 mM helpful.
Where stickiness of the fusion protein is a problem we recommend adding Tween 20 at a final concen-tration of 0.05% to 0.1%. At this concentration Tween 20 does not affect the performance of the CLIP-tag. Ionic detergents (e.g. SDS) should be avoided.
The maximum degree of labeling possible with the CLIP-tag is one molecule of label per molecule of fusion protein.
If exhaustive labeling of a protein sample is not achieved using the recommended conditions, try the following protocol modifications: Double the incubation time to two hours total at 25°C or to 24 hours at 4°C; or double the ratio of label to protein in the labeling reaction. Both approaches may be combined. If you still have poor labeling results, we recommend checking the activity of the CLIP-tag.
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.
DMSO at greater than 1% of the volume of protein solution may slow the reaction rate. Lower substrate concentrations also slow the reaction rate. Increasing the reaction time may be helpful in these cases.
Activity of the CLIP-tag can sometimes be partially or completely lost. This can be caused by extended storage of non-reacted CLIP-tag fusion proteins at 4°C or greater. The sensitivity of the CLIP-tag to inactivation is also significantly increased if no reducing agent is added.
If you believe that the activity of the CLIP-tag is affected, we recommend analyzing a small fraction of it on an SDS-PAGE gel using the CLIP-Vista Green (NEB #S9235S
) to confirm that the CLIP-tag is active.
If you encounter problems with the activity we rec-ommend thawing another sample of your protein or reexpressing and repurifying the CLIP-tag fusion protein following the advice given in the CLIP-tag plasmid instructions.