{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["35(12)"],"submitter":["Huang X"],"funding":["Regeneron Pharmaceuticals"],"pubmed_abstract":["Cysteine residues are crucial for the formation of conserved disulfide bonds in therapeutic monoclonal antibodies (mAbs), which are essential for their folding and structural stability. The presence of free thiols in mAbs can indicate incomplete disulfide bond formation, potentially impacting the molecule's conformational stability. Free thiol quantitation has been achieved using labeling-based strategies such as maleimide and haloalkyl derivatives at both intact and peptide levels. However, intact-level measurement only provides total free thiol levels, while peptide-level measurement is time-consuming and more prone to assay-induced artifacts. In this study, we present a novel label-free HILIC-MS method that separates free thiol species at the subunit level, followed by free thiol locali"],"journal":["Journal of the American Society for Mass Spectrometry"],"pagination":["3019-3027"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC11622229"],"repository":["biostudies-literature"],"pubmed_title":["Development of a Novel Label-Free Subunit HILIC-MS Method for Domain-Specific Free Thiol Identification and Quantitation in Therapeutic Monoclonal Antibodies."],"pmcid":["PMC11622229"],"pubmed_authors":["Qiu H","Wang S","Huang X","Bramhall D","Wang X","Zhong J","Cotham VC","Zhao Y","Li N"],"additional_accession":[]},"is_claimable":false,"name":"Development of a Novel Label-Free Subunit HILIC-MS Method for Domain-Specific Free Thiol Identification and Quantitation in Therapeutic Monoclonal Antibodies.","description":"Cysteine residues are crucial for the formation of conserved disulfide bonds in therapeutic monoclonal antibodies (mAbs), which are essential for their folding and structural stability. The presence of free thiols in mAbs can indicate incomplete disulfide bond formation, potentially impacting the molecule's conformational stability. Free thiol quantitation has been achieved using labeling-based strategies such as maleimide and haloalkyl derivatives at both intact and peptide levels. However, intact-level measurement only provides total free thiol levels, while peptide-level measurement is time-consuming and more prone to assay-induced artifacts. In this study, we present a novel label-free HILIC-MS method that separates free thiol species at the subunit level, followed by free thiol locali","dates":{"release":"2024-01-01T00:00:00Z","publication":"2024 Dec","modification":"2025-04-21T21:55:48.494Z","creation":"2025-04-21T21:55:48.494Z"},"accession":"S-EPMC11622229","cross_references":{"pubmed":["39476495"],"doi":["10.1021/jasms.4c00308"]}}