Designing potent antimicrobial peptides by disulphide linked dimerization and N-terminal lipidation to increase antimicrobial activity and membrane perturbation: Structural insights into lipopolysaccharide binding
Keywords: AMP; antimicrobial peptide; LPS; lipopolysachharide; MDR; multidrug resistance; trNOESY; Transferred Nuclear Overhauser Effect Spectroscopy; MIC; minimal inhibitory concentration; Antimicrobial peptide; Peptide modifications; Antibacterial activity; Membr