Difference between revisions of "Part:BBa K2548008"
 
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An antimicrobial peptide that is not homologous to any AMPs currently known, cPcAMP1, is identified from Ciliata Paramecium Caudatum and is able to A. hydrophila. More importantly, it’s able to induce bacterial membrane permeabilization and depolarization, and it’s not cytotoxic to mammalian cells.  
 
An antimicrobial peptide that is not homologous to any AMPs currently known, cPcAMP1, is identified from Ciliata Paramecium Caudatum and is able to A. hydrophila. More importantly, it’s able to induce bacterial membrane permeabilization and depolarization, and it’s not cytotoxic to mammalian cells.  
  
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<h2>Characterization</h2>
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<p>We examined the length of protein we extracted by performing SDS-PAGE to the supernatant after ultrasonic lysis. The protein size of  is 11.54 kDa. Protein band in the correct molecular weight range were visualized in the area between 15 kDa and 10 kDa. There was no protein band in the same area for control group, indicating that cPcAMP1 was successfully expressed. </p>
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[[Image:Proteingel.png|thumb|center|400px|Fig.1 Protein bands of antimicrobial peptides]]<br>
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<p>We tested the effect of different antimicrobial peptides through the procedures described in Experiments. The photo below show Aeromonas hydrophila under electron microscope. </p>
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[[Image: AMAMP.png|thumb|center|600px|Fig.2 Cells of A.hydrophila processed by cPcAMP1]]<br>
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<p>Figure 2 shows a group of broken A.hydrophila that has been processed by cPcAMP1. The edges of the cells are clearly rougher than those of cells in the control group, with some obvious light leaves as circled in blue. We suppose the darkened parts among and besides the cells (circled in red) are the cell structures flowed out of the cell via the gaps on cell walls. </p>
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<p>Through the electron microscope photos, we could demonstrate that our cPcAMP1 solution caused damage on cell walls of A.hydrophila. </p>
  
 
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Latest revision as of 22:28, 17 October 2018


cPcAMP1


An antimicrobial peptide that is not homologous to any AMPs currently known, cPcAMP1, is identified from Ciliata Paramecium Caudatum and is able to A. hydrophila. More importantly, it’s able to induce bacterial membrane permeabilization and depolarization, and it’s not cytotoxic to mammalian cells.

Characterization

We examined the length of protein we extracted by performing SDS-PAGE to the supernatant after ultrasonic lysis. The protein size of is 11.54 kDa. Protein band in the correct molecular weight range were visualized in the area between 15 kDa and 10 kDa. There was no protein band in the same area for control group, indicating that cPcAMP1 was successfully expressed.

Fig.1 Protein bands of antimicrobial peptides

We tested the effect of different antimicrobial peptides through the procedures described in Experiments. The photo below show Aeromonas hydrophila under electron microscope.

Fig.2 Cells of A.hydrophila processed by cPcAMP1


Figure 2 shows a group of broken A.hydrophila that has been processed by cPcAMP1. The edges of the cells are clearly rougher than those of cells in the control group, with some obvious light leaves as circled in blue. We suppose the darkened parts among and besides the cells (circled in red) are the cell structures flowed out of the cell via the gaps on cell walls.

Through the electron microscope photos, we could demonstrate that our cPcAMP1 solution caused damage on cell walls of A.hydrophila.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]