Weizmann Institute's Lipo-Isopeptides Kill Candida, Block Biofilms, and Resist Enzymes Better Than Standard Antimicrobial Peptides
Weizmann Institute of Science researchers reported in the Journal of Medicinal Chemistry on October 17, 2026 that adding isopeptide bonds and fatty-acid tails to antimicrobial peptides produced lipo-isopeptides that resisted breakdown by protein-cutting enzymes and were most active against the yeast Candida albicans. The lead compound, C8-Amp1EP, was non-toxic in their tests, reduced fungal attachment and biofilm formation when coated on surfaces and cells, disrupted the fungal membrane, and was less likely than standard antifungal drugs to select for resistance during repeated exposure. The work is in the lab.