Selenite mediated disulfide bond stabilization: BayerRecent Research Landscape
Host cell protein contamination risks batch rejection and immunogenicity in therapeutic biologics. These innovations engineer specific resin-ligand interactions to differentiate and isolate target antibodies from complex mammalian proteomes.
What technical problems is Bayer addressing in Selenite mediated disulfide bond stabilization?
Protein structural instability
(11)evidences
Unstable molecular structures lead to rapid degradation and loss of biological activity. Enhancing structural integrity through mediated bonding extends shelf life and therapeutic efficacy.
Insufficient therapeutic protein expression
(7)evidences
Restricted protospacer adjacent motif recognition and suboptimal delivery vehicle stability limit therapeutic efficacy. Enhancing specificity and payload integrity prevents off-target mutations and low protein expression.
Inadequate mucosal immune response
(2)evidences
The inability of the immune system to recognize and attack endogenous proteins or tumor antigens. Overcoming this biological barrier is necessary for effective cancer immunotherapy and autoimmune disease treatment.