4.8 Article

New Class of Heterogeneous Helical Peptidomimetics

Journal

ORGANIC LETTERS
Volume 17, Issue 14, Pages 3524-3527

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.5b01608

Keywords

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Funding

  1. NSF [1351265]
  2. Division Of Chemistry
  3. Direct For Mathematical & Physical Scien [1351265] Funding Source: National Science Foundation

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A new class of unnatural heterogeneous foldamers is reported to contain alternative a-amino acid and sulfono-gamma-AA amino acid residues in a 1:1 repeat pattern. Two-dimensional NMR data show that two 1:1 alpha/sulfono-gamma-AA peptides with diverse side chains form analogous right-handed helical structures in solution. The effects of sequence length, side chain, N-capping, and temperature on folding. propensity were further investigated using circular dichroism and small-angle X-ray scattering.

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