Chiral Sulfoxide-Induced Single Turn Peptide α-Helicity

نویسندگان

  • Qingzhou Zhang
  • Fan Jiang
  • Bingchuan Zhao
  • Huacan Lin
  • Yuan Tian
  • Mingsheng Xie
  • Guoyun Bai
  • Adam M. Gilbert
  • Gilles H. Goetz
  • Spiros Liras
  • Alan A. Mathiowetz
  • David A. Price
  • Kun Song
  • Meihua Tu
  • Yujie Wu
  • Tao Wang
  • Mark E. Flanagan
  • Yun-Dong Wu
  • Zigang Li
چکیده

Inducing α-helicity through side-chain cross-linking is a strategy that has been pursued to improve peptide conformational rigidity and bio-availability. Here we describe the preparation of small peptides tethered to chiral sulfoxide-containing macrocyclic rings. Furthermore, a study of structure-activity relationships (SARs) disclosed properties with respect to ring size, sulfur position, oxidation state, and stereochemistry that show a propensity to induce α-helicity. Supporting data include circular dichroism spectroscopy (CD), NMR spectroscopy, and a single crystal X-ray structure for one such stabilized peptide. Finally, theoretical studies are presented to elucidate the effect of chiral sulfoxides in inducing backbone α-helicity.

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عنوان ژورنال:

دوره 6  شماره 

صفحات  -

تاریخ انتشار 2016