Difference between revisions of "Part:BBa K3187017"

Line 8: Line 8:
 
     <div class="col mx-2">
 
     <div class="col mx-2">
 
      
 
      
         <h3>Profile</h3>
+
         <h2>Profile</h2>
 
         <table style=“width:80%“>
 
         <table style=“width:80%“>
 
         <tr>
 
         <tr>
Line 23: Line 23:
 
         </tr>
 
         </tr>
 
         <tr>
 
         <tr>
         <td><b>Origin</b></td>
+
         <td><b>Origin</b>></td>
 
         <td>Bacteriophage P22</td>
 
         <td>Bacteriophage P22</td>
 
         </tr>
 
         </tr>
Line 54: Line 54:
 
                       capsid, it represents one main part of our Virus-like particle. Together with the scaffold protein  
 
                       capsid, it represents one main part of our Virus-like particle. Together with the scaffold protein  
 
                         <a href="https://parts.igem.org/Part:BBa_K3187021"target="_blank">(BBa_K3187021)</a>,  
 
                         <a href="https://parts.igem.org/Part:BBa_K3187021"target="_blank">(BBa_K3187021)</a>,  
                       they assemble to a VLP and form the basis for our modular platform.
+
                       they assemble to a VLP
 +
                      <sup id="cite_ref-3" class="reference">
 +
                          <a href="#cite_note-3">[3] </a>
 +
                        </sup>                     
 +
                      and form the basis for our modular platform.
 
                        
 
                        
 
                        
 
                        
Line 72: Line 76:
 
       a Short Linker 5AA <a href="https://parts.igem.org/Part:BBa_K3187030"target="_blank">(BBa_K3187030)</a>
 
       a Short Linker 5AA <a href="https://parts.igem.org/Part:BBa_K3187030"target="_blank">(BBa_K3187030)</a>
 
       and Strep-tagII<a href="https://parts.igem.org/Part:BBa_K3187025"target="_blank">(BBa_K3187025)</a>. The production is performed in the <i>E. coli</i>  strain BL21 (DE3)  
 
       and Strep-tagII<a href="https://parts.igem.org/Part:BBa_K3187025"target="_blank">(BBa_K3187025)</a>. The production is performed in the <i>E. coli</i>  strain BL21 (DE3)  
       and it is purified with <a href="#"target="_blank">GE Healthcare ÄTKA Pure machine</a>which is a machine for FPLC. To verify the successful production,   
+
       and it is purified with <a href="https://2019.igem.org/wiki/images/6/62/T--TU_Darmstadt--Methoden.pdf"target="_blank">GE Healthcare ÄTKA Pure machine</a>which is a machine for FPLC. To verify the successful production,   
 
       a Western blot is carried out.
 
       a Western blot is carried out.
 
     </p>
 
     </p>
Line 79: Line 83:
 
           <a href="https://parts.igem.org/Part:BBa_K3187000"target="_blank">BBa_K3187000</a> (coat protein with LPETGG)   
 
           <a href="https://parts.igem.org/Part:BBa_K3187000"target="_blank">BBa_K3187000</a> (coat protein with LPETGG)   
 
           <a href="https://parts.igem.org/Part:BBa_K3187001"target="_blank">BBa_K3187001</a> (coat protein).
 
           <a href="https://parts.igem.org/Part:BBa_K3187001"target="_blank">BBa_K3187001</a> (coat protein).
         The production is performed in <i>E. coli</i>BL21 and it is purified with <a herf="#"target="_blank">GE Healthcare ÄKTA Pure machine </a>
+
         The production is performed in <i>E. coli</i> BL21 and it is purified with  
 +
        <a herf="https://2019.igem.org/wiki/images/6/62/T--TU_Darmstadt--Methoden.pdf"target="_blank">GE Healthcare ÄKTA Pure machine </a>
 
         which  
 
         which  
 
         is a machine for FPLC.
 
         is a machine for FPLC.
         To verify the right production, a <a herf="#"target="_blank">Western blot</a> is made.
+
         To verify the right production, a <a herf="https://2019.igem.org/wiki/images/6/62/T--TU_Darmstadt--Methoden.pdf"target="_blank">Western blot</a> is made.
 
         <div style="text-align: center;">  
 
         <div style="text-align: center;">  
 
         <img class="img-fluid center" src="https://2019.igem.org/wiki/images/9/9c/T--TU_Darmstadt--Western_blot_CP-LPETGG_CP.jpeg" style="max-width:60%" />
 
         <img class="img-fluid center" src="https://2019.igem.org/wiki/images/9/9c/T--TU_Darmstadt--Western_blot_CP-LPETGG_CP.jpeg" style="max-width:60%" />
Line 109: Line 114:
 
                   Juan S. Bonifacino, Jennifer Lippincott-Schwartz, Coat proteins: shaping membranetransport,  
 
                   Juan S. Bonifacino, Jennifer Lippincott-Schwartz, Coat proteins: shaping membranetransport,  
 
                   NATURE REVIEWS MOLECULAR CELLBIOLOGY, May 2013, 4, 409-414
 
                   NATURE REVIEWS MOLECULAR CELLBIOLOGY, May 2013, 4, 409-414
                 <a rel="nofollow" class="external autonumber" href="#">[1] </a>
+
                 <a rel="nofollow" class="external autonumber" href="https://www.nature.com/articles/nrm1099">[1] </a>
 
                 </span>
 
                 </span>
 
               </li>
 
               </li>
Line 123: Line 128:
 
                       </span>
 
                       </span>
 
               </li>
 
               </li>
 +
              <li id="cite_note-3">
 +
                  <span class="mw-cite-backlink">
 +
                  <a href="#cite_ref-3">↑</a>
 +
                  </span>
 +
                  <span class="reference-text">
 +
                  W. Earnshaw, S. Casjens, S. C. Harrison, Assembly of the head of bacteriophage P22: X-ray
 +
                  diffraction
 +
                  from heads, proheads and related structures J. Mol. Biol. 1976, 104, 387.
 +
                  <a rel="nofollow" class="external autonumber" href="https://www.sciencedirect.com/science/article/pii/0022283676902783?via%3Dihub">[3] </a>
 +
                  </span>
 +
                  </li>
 
             </ol>
 
             </ol>
 
     </div>
 
     </div>

Revision as of 08:14, 17 October 2019


P22 Bacteriophage Coat Protein

Profile

Name Coat protein
Base pairs 1293
Molecular weigth 46.9 kDa
Origin> Bacteriophage P22
Parts Basic part
Properties Assembly with scaffold proteins to VLPs

Usage and Biology

Coat Protein is an umbrella term for many different proteins, which simplify the transfer of molecules between different compartments that are surrounded by a membrane. [1] We focused on the viral and bacteriophagic coat proteins, which are parts of their respective organisms’ capsid. The genetic information (DNA or RNA) is wrapped and protected by the capsid. During cell infection, the phage or virus transfer the genetic information into the infected cell. [2] Because of the high variety of coat proteins, we are focussing on one specific coat protein (BBa_K3187017), which is naturally found in the bacteriophage P22. This coat protein (CP) consists of 431 amino acids and its molecular weight is 46.9 kDa. Because of its significance as a part of the capsid, it represents one main part of our Virus-like particle. Together with the scaffold protein (BBa_K3187021), they assemble to a VLP [3] and form the basis for our modular platform.

Methods

The basic part coat protein is produced and purified as the composite part (BBa_K3187000) (CP-LPETGG) and (BBa_K3187001) (CP). For gene expression and protein purification as CP-LPETGG the coding sequence contains a coat protein (BBa_K3187017) a LPETGG (BBa_K3187019), a T7 promoter, lac-operator and RBS (BBa_K3187029), a Short Linker 5AA (BBa_K3187030) T7 terminator (BBa_K3187032), and Strep-tagII (BBa_K3187025). The composite part coat protein without LPETGG (BBa_K3187001) contains a T7 promoter, lac-operator and RBS (BBa_K3187029), two terminators (T7Te terminator and rrnb T1 terminator (BBa_K3187036)), a Short Linker 5AA (BBa_K3187030) and Strep-tagII(BBa_K3187025). The production is performed in the E. coli strain BL21 (DE3) and it is purified with GE Healthcare ÄTKA Pure machinewhich is a machine for FPLC. To verify the successful production, a Western blot is carried out.

Results

The basic part coat portein was expressed, produced and purified as the composite part BBa_K3187000 (coat protein with LPETGG) BBa_K3187001 (coat protein). The production is performed in E. coli BL21 and it is purified with GE Healthcare ÄKTA Pure machine which is a machine for FPLC. To verify the right production, a Western blot is made.

Figure 1: Western blot of all produced and purified proteins.

Fig. 1 shows that the band of the CP-LPETGG is approximately found by the 49 kDa band and the band of CP by 46.9 kDa. Consequently, the successful production was proven. CP-LPETGG and CP were detected with Strep-Tactin-HRP.

References

  1. Juan S. Bonifacino, Jennifer Lippincott-Schwartz, Coat proteins: shaping membranetransport, NATURE REVIEWS MOLECULAR CELLBIOLOGY, May 2013, 4, 409-414 [1]
  2. Sherwood Casjens and Peter Weigele, DNA Packaging by Bacteriophage P22, Viral Genome Packaging Machines: Genetics, Structure, and Mechanism, 2005, 80- 88 [2]
  3. W. Earnshaw, S. Casjens, S. C. Harrison, Assembly of the head of bacteriophage P22: X-ray diffraction from heads, proheads and related structures J. Mol. Biol. 1976, 104, 387. [3]
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]