Antimicrobial peptides: Difference between revisions
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In the Transmembrane Pore Models, it is suggested that AMPs form many pores in the mambrane, so that it cannot hold it's content anymore. | In the Transmembrane Pore Models, it is suggested that AMPs form many pores in the mambrane, so that it cannot hold it's content anymore. | ||
The''' transmembrane pore mechanism''' has 2 main models: | The''' transmembrane pore mechanism''' has 2 main models: | ||
'''1- barrel stave pore model''' ,that claims peptides interact laterally with one another to form a specific structure enclosing a water-filled channel, much like a protein ion channel. | '''1- barrel stave pore model''' ,that claims peptides interact laterally with one another to form a specific structure enclosing a water-filled channel, much like a protein ion channel. | ||
[[Image:Barrel stave pore model.JPG]] | [[Image:Barrel stave pore model.JPG]] | ||
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the '''Nonepore model''' claims peptides bind to the membrane until it collapses. It is devided into 2 main mechanisms: | the '''Nonepore model''' claims peptides bind to the membrane until it collapses. It is devided into 2 main mechanisms: | ||
'''1- The carpet model''': In this model, antimicrobial peptides accumulate on the membrane surface with an orientation that is parallel to the membrane.When peptide concentration has reached a critical level permeabilization occurs via global bilayer destabilization. | '''1- The carpet model''': In this model, antimicrobial peptides accumulate on the membrane surface with an orientation that is parallel to the membrane.When peptide concentration has reached a critical level permeabilization occurs via global bilayer destabilization. | ||
'''2- detergent model''' : collapse of membrane integrity, observed with some AMPs at high peptide concentration. | '''2- detergent model''' : collapse of membrane integrity, observed with some AMPs at high peptide concentration. | ||
[[Image:Detergent model.JPG]] | [[Image:Detergent model.JPG]] | ||