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. Author manuscript; available in PMC: 2023 May 9.
Published in final edited form as: Biochem Pharmacol. 2021 Jul 22;192:114693. doi: 10.1016/j.bcp.2021.114693

Fig. 7. Ponericins adopt an α-helical conformation in lipid-like environments.

Fig. 7.

CD spectra of synthetic ponericins (25 μM) dissolved in (A) ultrapure water, (B) 20% TFE, and (C) 20 mM SDS. Α-Helical wheel projections generated using NetWheels (35] for (D) Na1b; (E) Nc1a; (F) Nc2a; (G) Nc3a (N-tenninal, Gl-Pl8); (H) Nc3a CC-terminal El9-N30); and (I) Nc3b. Two wheels are shown for Nc3a representing the regions either side of a proline residue, which is likely to disrupt helicity.