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Understanding the molecular mechanisms of antimicrobial peptide–membrane interactions is crucial in predicting the design of useful synthetic antimicrobial peptide analogues. Defensins are small (3–5 kDa) cysteine-rich cationic proteins which constitute the front line of host innate immunity. In this study, a series of eight 10 AA C-terminal analogues of hBD3 [sequence: RGRKXXRRKK, X = W, F, Y, V,...
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