Robert Doerksen, a postdoctoral researcher in Penn's Department of Chemistry, will present how the Penn team successfully modified the arylamide-based polymers to be safe for contact with human cells today at the American Chemical Society's 227th National Meeting in Anaheim, Calif.
"Our original approach was to replace the peptide backbone found in magainin with one of arylamide, which is relatively easy to create in the lab," Doerksen said. "Like magainin, the modified arylamide polymer can disrupt the cell membranes of bacteria without harming the membranes of other types of cells, such as our own."
The key to both magainin and the arylamide polymers is that they are amphiphilic – one side attracts water while the other repels it. It is thought that this property of the material allows it to reach the bacterial cell membrane and induce leakage that destroys the bacteria. "Unlike conventional antibiotics, for example, the arylamide's ability to attack a fundamental feature of all types of bacteria, their lipid membranes, will make it much more difficult for bacteria to evolve resistance," Doerksen said.
Penn researchers involved in the study include Michael L. Klein of the Department of Chemistry and William F. DeGrado of the Department of Biochemistry and Biophysics. Bin Chen of Louisiana State University and Dahui Liu, of Polymedix, Inc. also were contributing researchers. The scientific computing was performed in part at the Pittsburgh Supercomputing Center.