ArticleThe journal of physical chemistry. B2026
Cyclodextrin and KR12-Lipopeptide Interactions: A Thermodynamic View of Binding Mechanisms and Impact on the Structure of α-Helical Peptides.
Article in The journal of physical chemistry. B, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Natural antimicrobial peptides are a promising new class of antibiotics that offer a potential response to the growing challenge of microbial resistance. Among these, lipopeptides─cationic peptides conjugated with fatty acid residues─are especially noteworthy as their tendency to form α-helical structures plays a crucial role in determining their biological effectiveness. The ability to adopt an ordered structure, which directly influences their antimicrobial action, is determined by the length of the conjugated alkyl chain. In this study, experimental methods (isothermal titration calorimetry and circular dichroism), complemented by in silico analysis, have been successfully applied to rigorously characterize the interactions between three types of cyclodextrin (α-, ß-, and γ-) and three variants of antimicrobial KR12-lipopeptides, namely, the octanoylated (C8-KR12-NH
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