Difference between revisions of "Part:BBa K5531009"
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+ | <title>BBa_K5531009 (pET-24a-EPG50-P8VP4)</title> | ||
+ | <style> | ||
+ | img { | ||
+ | max-width: 80%; /* Adjust this percentage to change size relative to text */ | ||
+ | height: auto; /* Maintain aspect ratio */ | ||
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+ | .caption { | ||
+ | text-align: center; | ||
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+ | margin-bottom: 20px; /* Space below the caption */ | ||
+ | } | ||
+ | </style> | ||
+ | </head> | ||
+ | <body> | ||
+ | <h2>BBa_K5531009 (pET-24a-EPG50-P8VP4)</h2> | ||
+ | |||
+ | <h3>Construction Design</h3> | ||
+ | <p> | ||
+ | Using the backbone of pET-24a (BBa_K5531005), proline-free heterotrimeric collagen-like protein motif EPG50 is fused with serological P8-VP4 via chemical synthesis. The homologous recombination method was employed for the construction of pET24a-EPG50-P8VP4 (BBa_K5531009). | ||
+ | </p> | ||
+ | |||
+ | <!-- Figure 1 --> | ||
+ | <div style="text-align:center;"> | ||
+ | <img src="https://static.igem.wiki/teams/5531/bba-k5531009/1.png" alt="Figure 1: Plasmid map of pET-24a-EPG50-P8VP4"> | ||
+ | <div class="caption">Fig. 1. Plasmid map of pET-24a-EPG50-P8VP4</div> | ||
+ | </div> | ||
+ | |||
+ | <h3>Experimental Approach</h3> | ||
+ | <p> | ||
+ | We isolated pET-24a vectors from bacterial solutions primarily by centrifugation. The vectors were then obtained from the remains in the absorption column. Subsequently, we linearized the vectors using restriction enzymes and conducted electrophoresis to analyze the products. The electrophoresis result displayed correctness toward the expected outcome (EPG50-P8VP4 is 2000 bp); we selected colonies and sent them directly for sequencing. Figure 2 shows the success of pET24a-EPG50-P8VP4 construction. | ||
+ | </p> | ||
+ | |||
+ | <!-- Figure 2 --> | ||
+ | <div style="text-align:center;"> | ||
+ | <img src="https://static.igem.wiki/teams/5531/bba-k5531009/2.png" alt="Figure 2: The results of pET24a-EPG50-P8VP4"> | ||
+ | <div class="caption">Fig. 2. The results of pET24a-EPG50-P8VP4</div> | ||
+ | </div> | ||
+ | |||
+ | <h3>Characterization/Measurement</h3> | ||
+ | <p> | ||
+ | Later, the plasmid pET-24a-EPG50-P8VP4 was transferred to <em>E. coli</em> DH5α to replicate. The extracted plasmid was transferred into <em>E. coli</em> BL21, which can help express His-EPG50-P8VP4. After the colony PCR of <em>E. coli</em> BL21 was finished and verified, the bacteria were cultured and treated with 0.2 mM IPTG, which can promote protein expression. After promoting the protein expression overnight, the protein was purified via His-tag Purification Resin and went through SDS-PAGE electrophoresis. The target protein EPG50-P8VP4 has a size of 67.5 kDa. | ||
+ | </p> | ||
+ | |||
+ | <!-- Figure 3 --> | ||
+ | <div style="text-align:center;"> | ||
+ | <img src="https://static.igem.wiki/teams/5531/bba-k5531009/3.png" alt="Figure 3: The expression of EPG50-P8VP4 using E. coli BL21."> | ||
+ | <div class="caption">Fig. 3. The expression of EPG50-P8VP4 using E. coli BL21.</div> | ||
+ | </div> | ||
+ | |||
+ | <h3>Characterization of Collagen Oligomers</h3> | ||
+ | <p> | ||
+ | Collagen of the C-D-E-VP4 complex (in a 1:1:1 ratio) was diluted to a concentration of 0.5 mg/mL and incubated at 37°C for 1 hour before undergoing native-PAGE and SEC analysis. As illustrated in Figure 4, the samples were divided into two distinct clusters: high-molecular-weight and low-molecular-weight states. Each cluster contained multiple bands, indicative of varying degrees of proline hydroxylation. Based on the construct design, we hypothesized that the high-molecular-weight clusters represented the trimer assemblies, while the low-molecular-weight clusters corresponded to the monomers. This hypothesis was confirmed by the SEC analysis, as depicted in Figure 4. The peaks for the C-D-E-VP4 complex also ranged from 0.5 to 0.8 CV, with the prominent peaks at 0.57 CV, 0.68 CV, 0.72 CV, and 0.77 CV, indicating a trimer at 0.57 CV and the other peaks corresponding to the monomers of C, D, and E. | ||
+ | </p> | ||
+ | |||
+ | <!-- Figure 4 --> | ||
+ | <div style="text-align:center;"> | ||
+ | <img src="https://static.igem.wiki/teams/5531/bba-k5531009/4.jpg" alt="Figure 4: Native-PAGE analysis of oligomeric states of collagen C-D-E complex."> | ||
+ | <div class="caption">Fig. 4. Native-PAGE analysis of oligomeric states of collagen C-D-E complex (left); Size exclusion chromatographic (SEC) analysis of oligomeric states of collagen C-D-E complex (right).</div> | ||
+ | </div> | ||
+ | |||
+ | <h3>References</h3> | ||
+ | <p> | ||
+ | [1] Gauba V, Hartgerink JD. Self-assembled heterotrimeric collagen triple helices directed through electrostatic interactions. <em>J Am Chem Soc</em>. 2007 Mar 7;129(9):2683-90.<br> | ||
+ | [2] Liu Zezhong; Zhou Jie; Zhu Yun; Lu Lu; Jiang Shibo; School of Basic Medical Sciences, Fudan University; Department of Pharmacology, School of Pharmacy, Fudan University; Institute of Biophysics, Chinese Academy of Sciences. | ||
+ | </p> | ||
+ | |||
+ | </body> | ||
+ | </html> |
Revision as of 10:42, 29 September 2024
pET-24a-EPG50-P8VP4
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 5062
Illegal NotI site found at 5120 - 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 4957
Illegal BamHI site found at 5095
Illegal XhoI site found at 5129 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 137
Illegal NgoMIV site found at 3177
Illegal NgoMIV site found at 3337
Illegal NgoMIV site found at 4925 - 1000COMPATIBLE WITH RFC[1000]
<!DOCTYPE html>
BBa_K5531009 (pET-24a-EPG50-P8VP4)
Construction Design
Using the backbone of pET-24a (BBa_K5531005), proline-free heterotrimeric collagen-like protein motif EPG50 is fused with serological P8-VP4 via chemical synthesis. The homologous recombination method was employed for the construction of pET24a-EPG50-P8VP4 (BBa_K5531009).
Experimental Approach
We isolated pET-24a vectors from bacterial solutions primarily by centrifugation. The vectors were then obtained from the remains in the absorption column. Subsequently, we linearized the vectors using restriction enzymes and conducted electrophoresis to analyze the products. The electrophoresis result displayed correctness toward the expected outcome (EPG50-P8VP4 is 2000 bp); we selected colonies and sent them directly for sequencing. Figure 2 shows the success of pET24a-EPG50-P8VP4 construction.
Characterization/Measurement
Later, the plasmid pET-24a-EPG50-P8VP4 was transferred to E. coli DH5α to replicate. The extracted plasmid was transferred into E. coli BL21, which can help express His-EPG50-P8VP4. After the colony PCR of E. coli BL21 was finished and verified, the bacteria were cultured and treated with 0.2 mM IPTG, which can promote protein expression. After promoting the protein expression overnight, the protein was purified via His-tag Purification Resin and went through SDS-PAGE electrophoresis. The target protein EPG50-P8VP4 has a size of 67.5 kDa.
Characterization of Collagen Oligomers
Collagen of the C-D-E-VP4 complex (in a 1:1:1 ratio) was diluted to a concentration of 0.5 mg/mL and incubated at 37°C for 1 hour before undergoing native-PAGE and SEC analysis. As illustrated in Figure 4, the samples were divided into two distinct clusters: high-molecular-weight and low-molecular-weight states. Each cluster contained multiple bands, indicative of varying degrees of proline hydroxylation. Based on the construct design, we hypothesized that the high-molecular-weight clusters represented the trimer assemblies, while the low-molecular-weight clusters corresponded to the monomers. This hypothesis was confirmed by the SEC analysis, as depicted in Figure 4. The peaks for the C-D-E-VP4 complex also ranged from 0.5 to 0.8 CV, with the prominent peaks at 0.57 CV, 0.68 CV, 0.72 CV, and 0.77 CV, indicating a trimer at 0.57 CV and the other peaks corresponding to the monomers of C, D, and E.
References
[1] Gauba V, Hartgerink JD. Self-assembled heterotrimeric collagen triple helices directed through electrostatic interactions. J Am Chem Soc. 2007 Mar 7;129(9):2683-90.
[2] Liu Zezhong; Zhou Jie; Zhu Yun; Lu Lu; Jiang Shibo; School of Basic Medical Sciences, Fudan University; Department of Pharmacology, School of Pharmacy, Fudan University; Institute of Biophysics, Chinese Academy of Sciences.