| Autor: |
Wei B; Department of Chemistry and Biochemistry, University of California Los Angeles, Los Angeles, CA, USA. jloo@chem.ucla.edu., Zenaidee MA; Department of Chemistry and Biochemistry, University of California Los Angeles, Los Angeles, CA, USA. jloo@chem.ucla.edu.; Australian Proteome Analysis Facility, Macquarie University, Macquarie Park, NSW, Australia., Lantz C; Department of Chemistry and Biochemistry, University of California Los Angeles, Los Angeles, CA, USA. jloo@chem.ucla.edu., Williams BJ; Waters Corporation, Milford, MA, USA., Totten S; Waters Corporation, Milford, MA, USA., Ogorzalek Loo RR; Department of Chemistry and Biochemistry, University of California Los Angeles, Los Angeles, CA, USA. jloo@chem.ucla.edu., Loo JA; Department of Chemistry and Biochemistry, University of California Los Angeles, Los Angeles, CA, USA. jloo@chem.ucla.edu.; Department of Biological Chemistry, University of California Los Angeles, Los Angeles, CA, USA. |
| Abstrakt: |
Disulfide bonds in proteins have a substantial impact on protein structure, stability, and biological activity. Localizing disulfide bonds is critical for understanding protein folding and higher-order structure. Conventional top-down mass spectrometry (TD-MS), where only terminal fragments are assigned for disulfide-intact proteins, can access disulfide information, but suffers from low fragmentation efficiency, thereby limiting sequence coverage. Here, we show that assigning internal fragments generated from TD-MS enhances the sequence coverage of disulfide-intact proteins by 20-60% by returning information from the interior of the protein sequence, which cannot be obtained by terminal fragments alone. The inclusion of internal fragments can extend the sequence information of disulfide-intact proteins to near complete sequence coverage. Importantly, the enhanced sequence information that arise from the assignment of internal fragments can be used to determine the relative position of disulfide bonds and the exact disulfide connectivity between cysteines. The data presented here demonstrates the benefits of incorporating internal fragment analysis into the TD-MS workflow for analyzing disulfide-intact proteins, which would be valuable for characterizing biotherapeutic proteins such as monoclonal antibodies and antibody-drug conjugates. |
