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Photo-editable macromolecular information

Author

Listed:
  • Niklas Felix König

    (Université de Strasbourg, CNRS, Institut Charles Sadron UPR22)

  • Abdelaziz Al Ouahabi

    (Université de Strasbourg, CNRS, Institut Charles Sadron UPR22)

  • Laurence Oswald

    (Université de Strasbourg, CNRS, Institut Charles Sadron UPR22)

  • Roza Szweda

    (Université de Strasbourg, CNRS, Institut Charles Sadron UPR22)

  • Laurence Charles

    (Institute of Radical Chemistry)

  • Jean-François Lutz

    (Université de Strasbourg, CNRS, Institut Charles Sadron UPR22)

Abstract

Light-induced alteration of macromolecular information plays a central role in biology and is known to influence health, aging and Darwinian evolution. Here, we report that light can also trigger sequence variations in abiotic information-containing polymers. Sequence-coded poly(phosphodiester)s were synthesized using four phosphoramidite monomers containing either photo-sensitive or photo-inert substituents. These monomers allow different sequence manipulations. For instance, using two light-cleavable monomers containing o-nitrobenzyl ether and o-nitroveratryl ether motifs, photo-erasable digital polymers were prepared. These polymers can be decoded by tandem mass spectrometry but become unreadable after UVA exposure. The opposite behavior, i.e. photo-revealable sequences, was obtained with polymers made of two isobaric monomers containing light-cleavable o-nitrobenzyl ether and light-inert p-nitrobenzyl ether substituents. Furthermore, when the latter two monomers were used in conjunction with a third monomer bearing a light-inert OH group, site-directed photo-mutations were induced in synthetic polymers. This was used herein to change the meaning of binary sequences.

Suggested Citation

  • Niklas Felix König & Abdelaziz Al Ouahabi & Laurence Oswald & Roza Szweda & Laurence Charles & Jean-François Lutz, 2019. "Photo-editable macromolecular information," Nature Communications, Nature, vol. 10(1), pages 1-9, December.
  • Handle: RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-11566-2
    DOI: 10.1038/s41467-019-11566-2
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