Spider prey-wrapping silk is an α-helical coiled-coil/β-sheet hybrid nanofiber

Chem Commun (Camb). 2018 Sep 20;54(76):10746-10749. doi: 10.1039/c8cc05246h.

Abstract

Solid-State NMR results on 13C-Ala/Ser and 13C-Val enriched Argiope argentata prey-wrapping silk show that native, freshly spun aciniform silk nanofibers are dominated by α-helical (∼50% total) and random-coil (∼35% total) secondary structures, with minor β-sheet nanocrystalline domains (∼15% total). This is the most in-depth study to date characterizing the protein structural conformation of the toughest natural biopolymer: aciniform prey-wrapping silks.

MeSH terms

  • Alanine / chemistry
  • Amino Acid Sequence
  • Animals
  • Carbon Isotopes
  • Carbon-13 Magnetic Resonance Spectroscopy
  • Fibroins / chemistry*
  • Nanofibers / chemistry*
  • Protein Conformation, alpha-Helical
  • Protein Conformation, beta-Strand
  • Serine / chemistry
  • Silk / chemistry*
  • Spiders / chemistry
  • Valine / chemistry

Substances

  • Carbon Isotopes
  • Silk
  • Serine
  • Fibroins
  • Valine
  • Alanine