| Literature DB >> 30475601 |
Jake Jaffe1, Kristin Wucherer1, Justin Sperry2, Qin Zou2, Qing Chang2, Mark A Massa2, Keshab Bhattacharya2, Sandeep Kumar2, Maire Caparon2, David Stead3, Paul Wright3, Anouk Dirksen2, Matthew B Francis1,4.
Abstract
Conjugate vaccines prepared with the cross-reactive material 197 (CRM197) carrier protein have been successful in the clinic and are of great interest in the field of immunotherapy. One route to preparing peptide-CRM197 conjugate vaccines involves an activation-conjugation strategy, effectively coupling lysine residues on the protein to cysteine thiolate groups on the peptide of interest using a heterobifunctional linker as an activation agent. This method has been found to result in two distinct populations of conjugates, believed to be the result of a conformational change of CRM197 during preparation. This report explores the factors that lead to this conformational change, pointing to a model in which the unintentional alkylation of histidine-21 by the activating agent promotes the "opening" of the monomeric protein. This exposes a new set of lysine residues that are modified by additional activation agents. Subsequent peptide ligation to these sites results in the two conformers. This is the first time that a specific chemical modification is demonstrated to induce a defined conformational change for this carrier protein. Importantly, alternative conditions and reagents have been found to minimize this effect, improving the conformational homogeneity of peptide-CRM197 conjugates.Entities:
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Year: 2018 PMID: 30475601 DOI: 10.1021/acs.bioconjchem.8b00661
Source DB: PubMed Journal: Bioconjug Chem ISSN: 1043-1802 Impact factor: 4.774