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The bacterial and fungal cell membranes are essential lipid bilayer structures that regulate the transport of molecules, maintain cellular integrity, and play roles in signal transduction and energy metabolism[5][7]. They differ from mammalian cell membranes in composition, with fungal membranes rich in ergosterol and bacterial membranes largely composed of phospholipids and, in Gram-negative bacteria, also an outer membrane with unique lipopolysaccharides[5][7][6]. Both are validated therapeutic targets for antimicrobial agents: drugs that disrupt their structure or biosynthetic pathways typically result in cell death or loss of pathogenicity[2][4][6][8]. However, the term "cell membrane" refers collectively to a structural feature, not a specific protein, enzyme, or molecular entity, therefore it is ambiguous and should be replaced with a specific molecule, biosynthetic pathway, or membrane protein where possible for structured target databases[2][4][6].
Fungal membrane-targeting drugs: Bind to ergosterol, disrupting membrane integrity and causing cell death (polyenes like Amphotericin B and nystatin)[4][6][8] Inhibit ergosterol biosynthesis (azoles); loss of membrane function[2][6] Inhibit glucan synthesis in membrane/wall interface (echinocandins)[2][4] Target phospholipid composition (mandimycin)[8] Bacterial membrane-targeting drugs: Disrupt ionic gradients and membrane permeability (polymyxins, daptomycin)
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