Innovative Zinc-Binding Inhibitors of Legionella pneumophila ProA π§ͺπ¦
These inhibitors target the zinc-dependent enzyme ProA π¬, a critical factor for the pathogenicity of Legionella pneumophila. Here's how they work:
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Reduced Collagen and Flagellin Degradation π️❌
By inhibiting ProA, these molecules prevent the breakdown of collagen π§± and flagellin π, key components targeted by the bacteria for host invasion.
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TLR5 Evasion Blocked π«π‘️
The inhibitors restore flagellin’s ability to activate TLR5 π, a receptor crucial for detecting bacterial invaders, ensuring an effective immune response π€Ί.
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Human Lung Tissue Protection π«πͺ
These inhibitors significantly reduce inflammation π₯ in lung tissues, curbing damage caused by bacterial infection and promoting healing πΏ.
This breakthrough paves the way for advanced treatments π₯ against bacterial infections, enhancing patient outcomes globally π.
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