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Notably, the PROTACs that have advanced into clinical studies are, in most cases, still based on this small-molecule design paradigm, rather than on macromolecular or biomacromolecular carrier systems

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The PfGrx C88S -catalyzed deglutathionylation of monothiol roGFP2 C208S (SSG) is therefore two orders of magnitudes faster than the glutathionylation of roGFP2 C208S (SH) by PfGrx C88S (SSG) (Table 1) corresponding to the strongly shifted equilibrium towards glutathionylated PfGrx C88S and reduced roGFP2 C208S in the redox mobility shift assays (Fig