4.6 Review

Application of the Inverse-Electron-Demand Diels-Alder Reaction for Metabolic Glycoengineering

Journal

FRONTIERS IN CHEMISTRY
Volume 9, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fchem.2021.654932

Keywords

inverse-electron-demand Diels-Alder reaction; carbohydrates; metabolic engineering; bioorthogonal chemistry; tetrazines

Funding

  1. Deutsche Forschungsgemeinschaft [SFB 969, SPP 1623]
  2. Ministerium fur Wissenschaft, Forschung und Kunst BadenWurttemberg [33-7533-7-11.9/7/2]
  3. COST Action GLYCONanoProbes [CA18132]

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The IEDDA reaction is a bioorthogonal ligation reaction that is emerging as a versatile tool in metabolic glycoengineering. It allows for the introduction of unnatural sugar derivatives with chemical reporter groups into cellular glycans, enabling visualization or isolation of glycoconjugates.
The inverse electron-demand Diels-Alder (IEDDA or DA(inv)) reaction is an emerging bioorthogonal ligation reaction that finds application in all areas of chemistry and chemical biology. In this review we highlight its application in metabolic glycoengineering (MGE). MGE is a versatile tool to introduce unnatural sugar derivatives that are modified with a chemical reporter group into cellular glycans. The IEDDA reaction can then be used to modify the chemical reporter group allowing, for instance, the visualization or isolation of glycoconjugates. During the last years, many different sugar derivatives as well as reporter groups have been published. These probes are summarized, and their chemical and biological properties are discussed. Furthermore, we discuss examples of MGE and subsequent IEDDA reaction that highlight its suitability for application within living systems.

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