Proteomics Core Facility

This facility provides a full proteomics infrastructure for the identification and characterisation of proteins.


Gel staining prior to protein identification

We accept samples for protein identification from coomassie gels.

Coomassie staining

Not all coomassie stains are compatible with mass spectrometry. We strongly recommend that you mix your own coomassie stains (see protocol below for the recipe).

We also do not accept gels that have been boiled or microwaved to speed up the staining or destaining process. Please never use overhead projector foils for gel scanning as this prevents the gel from being used for MS experiments.

Cutting of gel bands

If you have gels from which you like individual bands to be identified by MS, you have two options. First, you can send (or bring) the gel to the facility, and we cut out the band(s) that you indicate.

Alternatively, you can cut out gel bands yourself. In this second scenario, please take precautions to prevent contamination (keratins, etc).

Mass determination of intact proteins

The molecular mass of proteins is best determined under denaturing conditions. Please observe the following guidelines for sample preparation:

  • Provide at least 10 µL of a protein at a concentration of >1 mg/ml
  • No detergents in the buffer or during the purification
  • Samples should contain less than 5% glycerol
  • Proteins should be as pure as possible — we can measure simple mixtures of a few proteins or where both a modified and non-modified version of the protein exist, but not complex mixtures
  • A gel picture can be sent to PCF staff ahead of a request to evaluate whether the sample is pure enough for a successful analysis