Abstract
We report the synthesis and the functional studies of multiple crown alpha-helical peptides designed to form artificial ion channels. The approach combines the versatility of solid phase peptide synthesis, the conformational predictability of peptidic molecules, and the solution synthesis of crown ethers with engineerable ion-binding abilities. Several biophysical methods were employed to characterize the activity and the mode of action of these crown peptide nanostructures. The 21 residue peptides bearing six 21-EC-7 turned out to facilitate the translocation of ions in a similar fashion to natural ion channels.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Breast Neoplasms / metabolism
-
Breast Neoplasms / pathology
-
Cell Division / drug effects
-
Crown Ethers / chemical synthesis*
-
Crown Ethers / metabolism
-
Female
-
Humans
-
Ion Channels / chemical synthesis*
-
Ion Channels / chemistry
-
Ion Channels / metabolism*
-
Leukemia / metabolism
-
Leukemia / pathology
-
Lipid Bilayers / metabolism*
-
Membranes, Artificial
-
Microbial Sensitivity Tests
-
Models, Molecular
-
Peptide Fragments / chemical synthesis*
-
Peptide Fragments / chemistry
-
Peptide Fragments / physiology*
-
Phosphatidylcholines / metabolism
-
Protein Conformation
-
Structure-Activity Relationship
-
Tumor Cells, Cultured
Substances
-
Crown Ethers
-
Ion Channels
-
Lipid Bilayers
-
Membranes, Artificial
-
Peptide Fragments
-
Phosphatidylcholines