Artificial Zymogen Based on Protein–Polymer Hybrids

This study explores the synthesis and application of artificial zymogens using protein-polymer hybrids to mimic the controlled enzyme activation observed in natural zymogens. Pro-trypsin (pro-TR) and pro-chymotrypsin (pro-CT) hybrids were engineered by modifying the surfaces of trypsin (TR) and chymotrypsin (CT) with cleavable peptide inhibitors utilizing surface-initiated atom transfer radical polymerization. These hybrids exhibited 70 and 90% reductions in catalytic efficiency for pro-TR and pro-CT, respectively, due to the inhibitory effect of the grafted peptide inhibitors. The activation of pro-TR by CT and pro-CT by TR resulted in 1.5- and 2.5-fold increases in enzymatic activity, respectively. Furthermore, the activated hybrids triggered an enzyme activation cascade, enabling amplification of activity through a dual pro-protease hybrid system. This study highlights the potential of artificial zymogens for therapeutic interventions and biodetection platforms by harnessing enzyme activation cascades for precise control of catalytic activity.

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Publication Details

Journal
Biomacromolecules
Published
2024-10-18
DOI
https://doi.org/10.1021/acs.biomac.4c01079
Citations
5
Primary Topic
Advanced Polymer Synthesis and Characterization
Type
article
Field-Weighted Citation Impact
1.25

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article

Artificial Zymogen Based on Protein–Polymer Hybrids

Hironobu Murata, Bibifatima Kaupbayeva, Jonathan S. Dordick, Kriti Kapil, Krzysztof Aleksander Matyjaszewski, Alan J. Russell
article en
5 citations

Abstract

This study explores the synthesis and application of artificial zymogens using protein-polymer hybrids to mimic the controlled enzyme activation observed in natural zymogens. Pro-trypsin (pro-TR) and pro-chymotrypsin (pro-CT) hybrids were engineered by modifying the surfaces of trypsin (TR) and chymotrypsin (CT) with cleavable peptide inhibitors utilizing surface-initiated atom transfer radical polymerization. These hybrids exhibited 70 and 90% reductions in catalytic efficiency for pro-TR and pro-CT, respectively, due to the inhibitory effect of the grafted peptide inhibitors. The activation of pro-TR by CT and pro-CT by TR resulted in 1.5- and 2.5-fold increases in enzymatic activity, respectively. Furthermore, the activated hybrids triggered an enzyme activation cascade, enabling amplification of activity through a dual pro-protease hybrid system. This study highlights the potential of artificial zymogens for therapeutic interventions and biodetection platforms by harnessing enzyme activation cascades for precise control of catalytic activity.

BiomacromoleculesVol. 25(11)
Amgen (United States) (US), Rensselaer Polytechnic Institute (US), Department of Biotechnology (IN), South Eastern Europe Telecommunications Academy (GR), Nazarbayev University (KZ), Carnegie Mellon University (US)
National Science Foundation, Defense Threat Reduction Agency, Division of Materials Research
Zero hunger
Openalex Percentile: Top 22%
Advanced Polymer Synthesis and Characterization
1.25
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