Enzyme‐Based Synthetic Protein Nanoparticles as Colloidal Antioxidants

Author:

Mauser Ava12,Quevedo Daniel F.12,Zhang Boya234,Hernandez Yazmin12,Berardi Anthony25,Brown William26,Lee Sophia26,Miki Rikako12,Raymond Jeffery26,Lahann Joerg1256,Greineder Colin F.234

Affiliation:

1. Department of Biomedical Engineering University of Michigan Ann Arbor MI 48109 USA

2. Biointerfaces Institute University of Michigan Ann Arbor MI 48109 USA

3. Department of Emergency Medicine Department University of Michigan Ann Arbor MI 48109 USA

4. Pharmacology Department University of Michigan Ann Arbor MI 48109 USA

5. Macromolecular Science and Engineering University of Michigan Ann Arbor MI 48109 USA

6. Department of Chemical Engineering University of Michigan Ann Arbor MI 48109 USA

Abstract

AbstractProtein‐based drug delivery systems have gained popularity due to their biocompatibility, straightforward surface modification, and potential for intrinsic therapeutic activity. Among therapeutic proteins, enzymes are particularly attractive because of their specificity, efficient reaction rates, regeneration after substrate turnover, and proven track record in the treatment of diseases ranging from cancer to inherited metabolic and lysosomal storage disorders. Herein, previous work on electrohydrodynamic jetting is expanded upon by developing a novel class of protein nanoparticles that features therapeutic enzymes. In particular, nanoparticles incorporating the antioxidant enzyme, catalase, at weight fractions as high as 50% are reported. Catalase‐based synthetic protein nanoparticles (CAT‐SPNPs) demonstrate sustained antioxidative activity, retain significantly enhanced enzymatic activity compared to its solute form, and overall demonstrate good structural stability. Moreover, surface functionalization of CAT‐SPNPs with targeting antibodies results in ≈12.5‐fold increase in uptake over unmodified control particles. Importantly, CAT‐SPNPs exert protection from oxidative stress, as indicated by significant increase in viability and reduction in LDH release compared to equivalent amounts of free catalase. Taken together, the work establishes targeted enzyme‐based SPNPs as a platform for enhancing the drug‐like properties of therapeutic enzymes.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Pharmacology (medical),Biochemistry (medical),Genetics (clinical),Pharmaceutical Science,Pharmacology,Medicine (miscellaneous)

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