Tetracycline selectively targets prokaryotic cells because it binds to the 30S ribosomal subunit, inhibiting protein synthesis specific to bacteria. Prokaryotic ribosomes differ structurally from eukaryotic ribosomes, which have a 40S and 60S subunit composition. This structural distinction allows tetracycline to effectively disrupt bacterial translation while leaving eukaryotic cells largely unaffected. Consequently, tetracycline is a useful antibiotic for treating bacterial infections without harming the host's eukaryotic cells.
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