In a project, I am required to degrade proteins to a size of 10Kd. This would prevent protein from passing through ultrafiltration and being absent in the resultant. I suggested using SDS, however, I have been advised that SDS will not degrade proteins small enough.
In my lab, I was told to use a strong acid to hydrolyse the peptide bonds, but i think this will interfere with plastic polymers that i am trying to study
Any suggestions