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Intracellular Activation of Bioorthogonal Nanozymes through Endosomal Proteolysis of the Protein Corona.


ABSTRACT: Bioorthogonal activation of prodrugs provides a strategy for on-demand on-site production of therapeutics. Intracellular activation provides a strategy to localize therapeutics, potentially minimizing off-target effects. To this end, nanoparticles embedded with transition metal catalysts (nanozymes) were engineered to generate either "hard" irreversible or "soft" reversible coronas in serum. The hard corona induced nanozyme aggregation, effectively inhibiting nanozyme activity, whereas only modest loss of activity was observed with the nonaggregating soft corona nanozymes. In both cases complete activity was restored by treatment with proteases. Intracellular activity mirrored this reactivation: endogenous proteases in the endosome provided intracellular activation of both nanozymes. The role of intracellular proteases in nanozyme reactivation was verified through treatment of the cells with protease inhibitors, which prevented reactivation. This study demonstrates the use of intracellular proteolysis as a strategy for localization of therapeutic generation to within cells.

SUBMITTER: Zhang X 

PROVIDER: S-EPMC8297610 | biostudies-literature | 2020 Apr

REPOSITORIES: biostudies-literature

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Intracellular Activation of Bioorthogonal Nanozymes through Endosomal Proteolysis of the Protein Corona.

Zhang Xianzhi X   Liu Yuanchang Y   Gopalakrishnan Sanjana S   Castellanos-Garcia Laura L   Li Gengtan G   MalassinĂ© Morgane M   Uddin Imad I   Huang Rui R   Luther David C DC   Vachet Richard W RW   Rotello Vincent M VM  

ACS nano 20200407 4


Bioorthogonal activation of prodrugs provides a strategy for on-demand on-site production of therapeutics. Intracellular activation provides a strategy to localize therapeutics, potentially minimizing off-target effects. To this end, nanoparticles embedded with transition metal catalysts (nanozymes) were engineered to generate either "hard" irreversible or "soft" reversible coronas in serum. The hard corona induced nanozyme aggregation, effectively inhibiting nanozyme activity, whereas only mode  ...[more]

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