4.6 Article

Installing Reduction Responsiveness into Biomolecules by Introducing Nitroaryl Groups

Journal

CHEMISTRY-A EUROPEAN JOURNAL
Volume 28, Issue 48, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.202201103

Keywords

biomolecules; folding; nitroaryl group; reduction; self-assembly; stimuli-responsiveness

Funding

  1. JSPS [20J11206]
  2. CCI research grant
  3. iGCORE collaboration grant
  4. Grants-in-Aid for Scientific Research [20J11206] Funding Source: KAKEN

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Artificially synthesized stimuli-responsive biomolecules are attractive molecular tools for monitoring and modulating biological systems. This Concept article reviews the molecular design of reduction-responsive biomolecules, such as peptides, nucleic acids, and saccharides, produced by introducing nitroaryl groups into them, with a special emphasis on simple 4-nitrobenzene-based motifs.
Artificially synthesized stimuli-responsive biomolecules are attractive as molecular tools for monitoring and modulating biological systems. In biological systems, redox stimuli are common, and their dysregulation is typically linked to various abnormal or disease states. In this Concept article, the molecular design of reduction-responsive biomolecules, such as peptides, nucleic acids, and saccharides, which are produced by introducing nitroaryl groups into them, is reviewed with a special emphasis on simple 4-nitrobenzene-based motifs.

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