Connecting Hydrophobic Surfaces in Cyclic Peptides Increases Membrane Permeability.

Hoang, Huy N.; Hill, Timothy A.; Fairlie, David P.

N‐ or C‐methylation in natural and synthetic cyclic peptides can increase membrane permeability, but it remains unclear why this happens in some cases but not others. Here we compare three‐dimensional structures for cyclic peptides from six families, including isomers differing only in the location of an N‐ or Cα‐methyl substituent. We show that a single methyl group only increases membrane permeability when it connects or expands hydrophobic surface patches. Positional isomers, with the same molecular weight, hydrogen bond donors/acceptors, rotatable bonds, calculated LogP, topological polar surface area, and total hydrophobic surface area, can have different membrane permeabilities that correlate with the size of the largest continuous hydrophobic surface patch. These results illuminate a key local molecular determinant of membrane permeability.

CYCLIC peptides; MEMBRANE permeability (Biology); HYDROPHOBIC surfaces; PEPTIDOMIMETICS; STRUCTURAL isomers; MOLECULAR weights

Angewandte Chemie, 2021, Vol 133, Issue 15, p8466

0044-8249

Academic Journal

10.1002/ange.202012643