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Microbial cell membranes and surface macromolecules are essential structural and functional components that define the boundary of microorganisms and mediate their interaction with the environment. These targets include the cytoplasmic membrane, the outer membrane of Gram-negative bacteria, and various associated polymers such as peptidoglycan, lipopolysaccharides (LPS), and ergosterol (StatPearls, 2023). They play critical roles in maintaining osmotic pressure, facilitating selective transport, and providing scaffolds for signal transduction and cell wall synthesis. In the context of infectious diseases, these structures are vital for pathogen survival and virulence, making them highly effective targets for various classes of antibiotics and antifungals (NIH, 2022). For example, polymyxins act by binding to LPS and disrupting the outer membrane, while daptomycin causes rapid depolarization of the bacterial membrane (PubMed, 2021). Polyene antifungals like amphotericin B target ergosterol to create lethal pores in fungal membranes. Despite their efficacy, drugs targeting these components must overcome challenges such as host cell toxicity—due to similarities between microbial and mammalian membranes—and the increasing prevalence of antimicrobial resistance.
Disruption of membrane integrity, pore formation, inhibition of cell wall synthesis, and binding to specific surface lipids or proteins.
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