| Autor: |
Bisirri EA; Department of Chemical and Biological Engineering, University of Colorado, Boulder, Colorado 80309, United States., Wright TA; Department of Chemical and Biological Engineering, University of Colorado, Boulder, Colorado 80309, United States., Schwartz DK; Department of Chemical and Biological Engineering, University of Colorado, Boulder, Colorado 80309, United States., Kaar JL; Department of Chemical and Biological Engineering, University of Colorado, Boulder, Colorado 80309, United States. |
| Jazyk: |
angličtina |
| Zdroj: |
Biomacromolecules [Biomacromolecules] 2023 Sep 11; Vol. 24 (9), pp. 4033-4041. Date of Electronic Publication: 2023 Aug 23. |
| DOI: |
10.1021/acs.biomac.3c00396 |
| Abstrakt: |
Protein-polymer conjugation provides an opportune means to adjust the local environment of proteins and enhance protein stability, performance, and solubility. Although much attention has been focused on tuning protein-polymer interactions, the properties of polymer-modified proteins may also be altered by polymer-polymer interactions. Herein, we sought to better understand the influence of polymer-polymer interactions on Candida rugosa lipase, which was modified with random co-polymers composed of sulfobetaine methacrylate (SBMA) and poly(ethylene glycol) methacrylate (PEGMA). Our findings suggest that there is an apparent activity-stability tradeoff as a function of polymer composition. Specifically, as the ratio of SBMA to PEGMA increased, lipase stability was enhanced, whereas activity decreased. By tuning the monomer ratio, we showed that lipase productivity could be optimized. These findings are discussed in the context of complex enzyme-polymer and polymer-polymer interactions and ultimately may enable more informed conjugate designs and improved enzyme productivity in industrial biotransformations under harsh or extreme conditions. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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