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Reversibility and regioselectivity in thiol/disulfide interchange of tocinoic acid with glutathione in lyophilized solids

โœ Scribed by Lei Zhang; Todd D. Williams; Elizabeth M. Topp


Book ID
102394630
Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
120 KB
Volume
98
Category
Article
ISSN
0022-3549

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โœฆ Synopsis


Thiol/disulfide interchange is one of the most common routes of aggregation of lyophilized protein drug products, but the mechanisms of the reaction in the solid state have not been established. Here, we report perturbations in thiol/disulfide interchange upon lyophilization, using tocionic acid (cycloCYIQNC; TA(ox)) and glutathione (GSH) as model peptides. The results suggest that thiol/disulfide interchange reactions differ in aqueous solution and in dry lyophilized solids with regard to reversibility and regioselectivity. In solids, the reaction of TA(ox) with GSH is effectively irreversible and the less-hindered single mixed disulfide is formed exclusively.


๐Ÿ“œ SIMILAR VOLUMES


Thiol-disulfide interchange in the tocin
โœ Mette Thing; Jun Zhang; Jennifer Laurence; Elizabeth M. Topp ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 358 KB

Thiol-disulfide interchange (''disulfide scrambling'') is a common mechanism of covalent aggregation for protein drugs. Using tocinoic acid (cyclo-S-Cys-Tyr-Ile-Gln-Asn-Cys-(S); TA(ox)) and glutathione (gGlu-Cys-Gly; GSH), our previous work demonstrated that thiol/disulfide interchange is affected b