Difference between revisions of "Part:BBa K4140013"

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The Vesicular Stomatitis Virus G (VSV G) protein is a typical type III viral fusion protein that, when present in cell-free environments, forms complexes with plasmid DNA and particles that resemble MLV retroviruses and improves DNA transfection.
 
The Vesicular Stomatitis Virus G (VSV G) protein is a typical type III viral fusion protein that, when present in cell-free environments, forms complexes with plasmid DNA and particles that resemble MLV retroviruses and improves DNA transfection.
 
==Usage==
 
==Usage==
(VSV G) protein is a typical type III viral fusion protein that, considered the second component of SEND platform for RNA delivery we use it to deliver PAH mRNA to specific type of cells(hepatocyte) this will participate in decreasing the side effect and improving dose efficacy.
+
(VSV G) protein is a typical type III viral fusion protein that is considered the second component of SEND platform for RNA delivery we use it to deliver PAH mRNA to a specific type of cells(hepatocytes) this will participate in decreasing the side effect and improving dose efficacy as shown in figure 1.  
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[[Image:send.png|right| ]]
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Figure(1) SEND delivery to hepatocytes
  
 
==Characterization of Mutational Landscape==
 
==Characterization of Mutational Landscape==
  
After creating a multiple sequence alignment of the protein sequence and predicting mutational landscapes, the effect of these mutations on the evolutionary fitness of the protein is tested. The prediction of the mutational landscape by saturation mutagenesis of the VSVg-Fusogen protein. The (Y148H) mutation, as depicted in the chart, had the greatest score when compared to other mutations. On the other hand, it's clear that the (A56T) had the least evolutionary fitness for VSVg-Fusogen protein. As displayed in Figure(1)
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After creating a multiple sequence alignment of the protein sequence and predicting mutational landscapes, the effect of these mutations on the evolutionary fitness of the protein is tested. The prediction of the mutational landscape by saturation mutagenesis of the VSVg-Fusogen protein. The (Y148H) mutation, as depicted in the chart, had the greatest score when compared to other mutations. On the other hand, it's clear that the (A56T) had the least evolutionary fitness for VSVg-Fusogen protein. As displayed in Figure(2)
  
[[File:Vsvg.png|thumb|Right|Figure 1. (shows the mutational landscape of the VSVg-Fusogen protein.) ]]
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[[File:Vsvg.png|thumb|Right|Figure 2. (shows the mutational landscape of the VSVg-Fusogen protein.) ]]
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==Literature Characterization==
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In this study, HECA2 cells were infected with VSVIND at an MOI of 2 and cultured in the presence or absence of ammonium chloride Fig.1. At 24 hpi, the virus released from HECA2 cells was titrated by plaque assay in BHK-21 cells and expressed as PFU per cell. This study showed that ammonium chloride doesn’t affect virus yield.
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[[File:Vsvg-1.png|thumb|right|Figure 1. Treatment of HECA2 cells with NH4Cl]]
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[[File:Vsvg-2.png|thumb|left|Figure 2. Virus yield in different ammonium chloride concentration]]
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==Literature Characterization==
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In this study, HECA2 cells were infected with VSVIND at an MOI of 2 and cultured in the presence or absence of ammonium chloride Fig.1. At 24 hpi, the virus released from HECA2 cells was titrated by plaque assay in BHK-21 cells and expressed as PFU per cell. This study showed that ammonium chloride doesn’t affect virus yield as shown in figures 3 and 4.
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[[File:Vsvg-1.png|thumb|right|Figure 3. Treatment of HECA2 cells with NH4Cl]]
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[[File:Vsvg-2.png|thumb|left|Figure 4. Virus yield in different ammonium chloride concentration]]
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==References==
 
==References==

Latest revision as of 19:01, 11 October 2022


VSVg-Fusogen

Part Description

The Vesicular Stomatitis Virus G (VSV G) protein is a typical type III viral fusion protein that, when present in cell-free environments, forms complexes with plasmid DNA and particles that resemble MLV retroviruses and improves DNA transfection.

Usage

(VSV G) protein is a typical type III viral fusion protein that is considered the second component of SEND platform for RNA delivery we use it to deliver PAH mRNA to a specific type of cells(hepatocytes) this will participate in decreasing the side effect and improving dose efficacy as shown in figure 1.

Send.png

Figure(1) SEND delivery to hepatocytes

Characterization of Mutational Landscape

After creating a multiple sequence alignment of the protein sequence and predicting mutational landscapes, the effect of these mutations on the evolutionary fitness of the protein is tested. The prediction of the mutational landscape by saturation mutagenesis of the VSVg-Fusogen protein. The (Y148H) mutation, as depicted in the chart, had the greatest score when compared to other mutations. On the other hand, it's clear that the (A56T) had the least evolutionary fitness for VSVg-Fusogen protein. As displayed in Figure(2)

Figure 2. (shows the mutational landscape of the VSVg-Fusogen protein.)














Literature Characterization

In this study, HECA2 cells were infected with VSVIND at an MOI of 2 and cultured in the presence or absence of ammonium chloride Fig.1. At 24 hpi, the virus released from HECA2 cells was titrated by plaque assay in BHK-21 cells and expressed as PFU per cell. This study showed that ammonium chloride doesn’t affect virus yield as shown in figures 3 and 4.

Figure 3. Treatment of HECA2 cells with NH4Cl
Figure 4. Virus yield in different ammonium chloride concentration





























References

1. Roberts, P. C., Kipperman, T., & Compans, R. W. (1999). Vesicular stomatitis virus G protein acquires pH-independent fusion activity during transport in a polarized endometrial cell line. Journal of virology, 73(12), 10447-10457.‏ Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 1396
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal XhoI site found at 1176
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 987
  • 1000
    COMPATIBLE WITH RFC[1000]