Innovative Zinc-Binding Inhibitors of Legionella pneumophila ProA ๐งช๐ฆ
These inhibitors target the zinc-dependent enzyme ProA ๐ฌ, a critical factor for the pathogenicity of Legionella pneumophila. Here's how they work:
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Reduced Collagen and Flagellin Degradation ๐️❌
By inhibiting ProA, these molecules prevent the breakdown of collagen ๐งฑ and flagellin ๐, key components targeted by the bacteria for host invasion.
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TLR5 Evasion Blocked ๐ซ๐ก️
The inhibitors restore flagellin’s ability to activate TLR5 ๐, a receptor crucial for detecting bacterial invaders, ensuring an effective immune response ๐คบ.
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Human Lung Tissue Protection ๐ซ๐ช
These inhibitors significantly reduce inflammation ๐ฅ in lung tissues, curbing damage caused by bacterial infection and promoting healing ๐ฟ.
This breakthrough paves the way for advanced treatments ๐ฅ against bacterial infections, enhancing patient outcomes globally ๐.
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