All Stories

  1. A hydrophobic loop of the spider-venom peptide Tl1a drives activity at NaV1.8
  2. A venom peptide-induced NaV channel modulation mechanism involving the interplay between fixed channel charges and ionic gradients
  3. Evaluation of Peptide Ligation Strategies for the Synthesis of the Bivalent Acid-Sensing Ion Channel Inhibitor Hi1a
  4. Changes in Potency and Subtype Selectivity of Bivalent NaV Toxins are Knot-Specific
  5. Pain-causing stinging nettle toxins target TMEM233 to modulate NaV1.7 function
  6. µ-Conotoxins Targeting the Human Voltage-Gated Sodium Channel Subtype NaV1.7
  7. On the Utility of Chemical Strategies to Improve Peptide Gut Stability
  8. Structural and functional insights into inhibition of human voltage-gated sodium channels by μ‐conotoxin KIIIA disulfide isomers
  9. Evaluation of Efficient Non-reducing Enzymatic and Chemical Ligation Strategies for Complex Disulfide-Rich Peptides
  10. The Allosteric Activation of α7 nAChR by α-Conotoxin MrIC Is Modified by Mutations at the Vestibular Site
  11. Chemical Synthesis of TFF3 Reveals Novel Mechanistic Insights and a Gut-Stable Metabolite
  12. Improving the Gastrointestinal Stability of Linaclotide
  13. Discovery, Pharmacological Characterisation and NMR Structure of the Novel µ-Conotoxin SxIIIC, a Potent and Irreversible NaV Channel Inhibitor
  14. Manipulation of a spider peptide toxin alters its affinity for lipid bilayers and potency and selectivity for voltage-gated sodium channel subtype 1.7
  15. Enzymatic Ligation of a Pore Blocker Toxin and a Gating Modifier Toxin: Creating Double-Knotted Peptides with Improved Sodium Channel NaV1.7 Inhibition
  16. Novel heterodimeric ion channel modulators derived from conotoxins and spider toxins