4.8 Article

A tendril perversion in a helical oligomer: trapping and characterizing a mobile screw-sense reversal

Journal

CHEMICAL SCIENCE
Volume 8, Issue 4, Pages 3007-3018

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c6sc05474a

Keywords

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Funding

  1. ERC (Advanced Grant ROCOCO)
  2. EPSRC
  3. BBSRC
  4. EPSRC [EP/N009134/1, EP/L011999/1, EP/K03927X/1] Funding Source: UKRI
  5. Biotechnology and Biological Sciences Research Council [1575107] Funding Source: researchfish
  6. Engineering and Physical Sciences Research Council [EP/N009134/1, 1362087, EP/K03927X/1, EP/L011999/1] Funding Source: researchfish

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Helical oligomers of achiral monomers adopt domains of uniform screw sense, which are occasionally interrupted by screw-sense reversals. These rare, elusive, and fast-moving features have eluded detailed characterization. We now describe the structure and habits of a screw-sense reversal trapped within a fragment of a helical oligoamide foldamer of the achiral quaternary amino acid 2-aminoisobutyric acid (Aib). The reversal was enforced by compelling the amide oligomer to adopt a right-handed screw sense at one end and a left-handed screw sense at the other. The trapped reversal was characterized by X-ray crystallography, and its dynamic properties were monitored by NMR and circular dichroism, and modelled computationally. Raman spectroscopy indicated that a predominantly helical architecture was maintained despite the reversal. NMR and computational results indicated a stepwise shift from one screw sense to another on moving along the helical chain, indicating that in solution the reversal is not localised at a specific location, but is free to migrate across a number of residues. Analogous unconstrained screw-sense reversals that are free to move within a helical structure are likely to provide the mechanism by which comparable helical polymers and foldamers undergo screw-sense inversion.

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