Ouadhi Sara, López Dulce María Valdez, Mohideen F Ifthiha, Kwan David H
Centre for Applied Synthetic Biology, Concordia University, Montreal, QC H4B 2A6, Canada.
PROTEO, Quebec Network for Research on Protein Function, Structure, and Engineering, Quebec City, QC G1V 0A6, Canada.
Protein Eng Des Sel. 2023 Jan 21;36. doi: 10.1093/protein/gzac010.
Many glycosylated small molecule natural products and glycoprotein biologics are important in a broad range of therapeutic and industrial applications. The sugar moieties that decorate these compounds often show a profound impact on their biological functions, thus biocatalytic methods for controlling their glycosylation are valuable. Enzymes from nature are useful tools to tailor bioproduct glycosylation but these sometimes have limitations in their catalytic efficiency, substrate specificity, regiospecificity, stereospecificity, or stability. Enzyme engineering strategies such as directed evolution or semi-rational and rational design have addressed some of the challenges presented by these limitations. In this review, we highlight some of the recent research on engineering enzymes to tailor the glycosylation of small molecule natural products (including alkaloids, terpenoids, polyketides, and peptides), as well as the glycosylation of protein biologics (including hormones, enzyme-replacement therapies, enzyme inhibitors, vaccines, and antibodies).
许多糖基化小分子天然产物和糖蛋白生物制品在广泛的治疗和工业应用中都很重要。修饰这些化合物的糖部分通常对其生物学功能有深远影响,因此控制其糖基化的生物催化方法很有价值。来自自然界的酶是定制生物产品糖基化的有用工具,但这些酶有时在催化效率、底物特异性、区域特异性、立体特异性或稳定性方面存在局限性。诸如定向进化或半理性和理性设计等酶工程策略已经解决了这些局限性带来的一些挑战。在这篇综述中,我们重点介绍了一些关于工程酶的最新研究,这些研究旨在定制小分子天然产物(包括生物碱、萜类化合物、聚酮化合物和肽)的糖基化,以及蛋白质生物制品(包括激素、酶替代疗法、酶抑制剂、疫苗和抗体)的糖基化。