Assigning disulfide bridges is an important component of the analytical strategy during recombinant protein production, for which mass spectrometry (MS) is an important technique. Venom proteins, such as the three-finger toxins, pose a particular challenge due to their complex arrangement of disulfide linkages.
At the Institute of Life Technologies, we are developing capabilities for straight forward, efficient disulfide bridge assignment in proteins using mass spectrometry, in particular, to enable the study of 'challenging' proteins such as venom proteins, which fail simple disulfide bridge assignment methods. The disulfide assignment strategy is highly dependent on the protein sequence and disulfide bonding pattern. Thus, to study a variety of proteins with challenging disulfide connectivities, the toolkit of techniques in this area at FTV is being developed. This includes sample preparation methods, such as chemical/enzymatic digestion and partial reduction and mass spectrometric techniques (using a QTOF) to fragment along the polypeptide backbone and/or break disulfide bridges, determine with high accuracy the masses and elucidate the disulfide structure.