In order to understand the role of divalent metal cations particularly Zn2+, Mg2+, and Ca2+ in endotoxin removal from clarified cell lysate solutions, the aggregation of endotoxins by these cations was explored in this work using dynamic light scattering, zeta potential analysis, and improved endotoxin assay. This work concludes that Zn2+ (as ZnSO4) optimally binds to and increases the hydrodynamic size of endotoxins compared to Mg2+ and Ca2+. A low polydispersity index value measured after cation addition indicates the presence of homogenously suspended supramolecular endotoxin particles which calls for a centrifugal separation step for complete endotoxin removal.
In order to understand the role of divalent metal cations particularly Zn2+, Mg2+, and Ca2+ in endotoxin removal from clarified cell lysate solutions, the aggregation of endotoxins by these cations was explored in this work using dynamic light scattering, zeta potential analysis, and improved endotoxin assay. This work concludes that Zn2+ (as ZnSO4) optimally binds to and increases the hydrodynamic size of endotoxins compared to Mg2+ and Ca2+. A low polydispersity index value measured after cation addition indicates the presence of homogenously suspended supramolecular endotoxin particles which calls for a centrifugal separation step for complete endotoxin removal.
