How To Optimize Your Results With Low MW Proteins

At extreme ends of the Molecular weight (MW) spectrum, regular SDS-PAGE and Western blotting techniques suffer from limitations: poor separation, signal reduction, or even a total absence of target bands.  Low MW proteins (<20 kDa) modifications can be employed when handling these proteins to improve their retention and resolution.

Use Tricine

In general, glycine gels are ideal for resolving any proteins that fall within the MW range of 30–250 kDa. However, Acrylamide gels based on a Tris-Tricine buffer system will greatly improve your chances of “seeing” your target band(s) if you are working below the 30 kDa range.

(You can find a recipe for a 15% Tricine gel in the 'Tricine Gel Recipe for Low MW Proteins' section.)

Why It Works

The difference in separation capabilities of glycine and tricine gels is attributed to the differing properties of the glycine and tricine compounds, such as their pK values and ionic mobility. Tricine is more optimal for the separation of low MW proteins because it “stacks” proteins into more uniform bands. A tricine based stacking layer shifts the upper stacking limit down to as low as 30 kDa for the first stack,1 preventing overloading at the interface between the gel layers.

Protein Transfer

As well as ensuring the optimum separation of low MW proteins, you also need to take care at the protein transfer stage. Low MW proteins are susceptible to “over transfer” – loss of sample due to lack of retention by the transfer membrane and/or too-rapid transfer.

Membrane Choice and Pore Size

Most labs have a preferred choice of Western blotting membrane, however PVDF is a better choice in the case of smaller, low MW proteins, due to its greater capacity to bind proteins. There are various membrane pore sizes on offer – opt for a smaller pore size to obtain better transfers of your low MW target proteins.

Transfer Conditions

In addition to membrane choice, factors such as transfer system, length, temperature, and buffer composition come into play when dealing with low MW proteins. In the case of small proteins, less is often more when it comes to transfer length and voltage. How much you should adjust these by will be down to the brand and model of the system being used.

Other Tips

Be aware some proteins will escape the dye front of the sample loading buffer. You can choose to soak your gel in an SDS-free buffer (or simply H2O) for 5 minutes prior to setting up your transfer. This helps to remove SDS, which coats small proteins and protein fragments in negative charges, increasing their rate of passage through the Western blot membrane.