Team:Hannover/Results Project/Heavy Metals/Expression
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<h1>Results / Heterologous Expression</h1><p class="text">To examine whether the T4MBP was heterologous expressed by plants, leaves of <i>Nicotiana tabacum</i> plants were injected with pORE-E3_2x25S_T4MBP containing <i>Rhizobium radiobacter</i>. After separation of the leaf extracts by SDS-PAGE, an immunostaining aimed to specifically detect the T4MBP´s internal FLAG-tag (Figure 1A). Attributed to the antibodie´s unspecifity, the T4MBP could not be detected in the plant leaf extracts. Hence, the T4MBP coding construct was transferred into the pASK plasmid adding an n-terminal Strep-tag and a c-terminal 6xHistidine-tag to the target protein. Based on the engineered pASK_T4MBP, the heterologous expression and detection of the T4MBP could be successfully achieved in the end.</p> | <h1>Results / Heterologous Expression</h1><p class="text">To examine whether the T4MBP was heterologous expressed by plants, leaves of <i>Nicotiana tabacum</i> plants were injected with pORE-E3_2x25S_T4MBP containing <i>Rhizobium radiobacter</i>. After separation of the leaf extracts by SDS-PAGE, an immunostaining aimed to specifically detect the T4MBP´s internal FLAG-tag (Figure 1A). Attributed to the antibodie´s unspecifity, the T4MBP could not be detected in the plant leaf extracts. Hence, the T4MBP coding construct was transferred into the pASK plasmid adding an n-terminal Strep-tag and a c-terminal 6xHistidine-tag to the target protein. Based on the engineered pASK_T4MBP, the heterologous expression and detection of the T4MBP could be successfully achieved in the end.</p> | ||
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- | <p class="text">As the host for heterologous T4MBP expression we chose the Origami2 cells to work with. This <i>E. coli</i> strain expresses huge amounts of cytosolic disulfide isomerase cytosolic and thus elevates the chance of disulfide formation for recombinant proteins. To improve the quality of proteins, furthermore, we lowered the expression temperatures to 16 °C.</p><li>Cloning the sequences relevant for metal binding into the <a href="" target="_blank">pASK plasmid</a></li | + | <p class="text">As the host for heterologous T4MBP expression we chose the Origami2 cells to work with. This <i>E. coli</i> strain expresses huge amounts of cytosolic disulfide isomerase cytosolic and thus elevates the chance of disulfide formation for recombinant proteins. To improve the quality of proteins, furthermore, we lowered the expression temperatures to 16 °C.</p> |
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+ | <h2>Labwork 2</h2><p class="text"><ul><li>Cloning the sequences relevant for metal binding into the <a href="" target="_blank">pASK plasmid</a></li><li>Induction of protein expression under adapted conditions.</i></li><ol><li>Lysis of bacteria cells and protein precipitation by TCA.</color></li><li>Preparation of protein samples and analysis by SDS-PAGE (VERWEIS).</li><li>Transfer of separated proteins onto a PVDF membrane and an immunostaining(VERWEIS)by an anti-6xHistidine-tag antibody.</li></ul></p> | ||
<h2>Results</h2> | <h2>Results</h2> |
Revision as of 23:33, 13 October 2014
Results / Heterologous Expression
To examine whether the T4MBP was heterologous expressed by plants, leaves of Nicotiana tabacum plants were injected with pORE-E3_2x25S_T4MBP containing Rhizobium radiobacter. After separation of the leaf extracts by SDS-PAGE, an immunostaining aimed to specifically detect the T4MBP´s internal FLAG-tag (Figure 1A). Attributed to the antibodie´s unspecifity, the T4MBP could not be detected in the plant leaf extracts. Hence, the T4MBP coding construct was transferred into the pASK plasmid adding an n-terminal Strep-tag and a c-terminal 6xHistidine-tag to the target protein. Based on the engineered pASK_T4MBP, the heterologous expression and detection of the T4MBP could be successfully achieved in the end.
Labwork 1
- Cloning the synthesized GeneArt construct into our pORE-E3_2x35S vector system
- Infiltration of Nicotiana tabacum leaves with pORE-E3_2x25S_T4MPB-containing Rhizobium radiobacter cells.
- Extraction of proteins from the leaf tissue and subsequent seperation via SDS-PAGE (VERWEIS).
- Transfer onto a PVDF membrane and immunostaining(VERWEIS)via anti-FLAG-tag antibody.
Results
As the host for heterologous T4MBP expression we chose the Origami2 cells to work with. This E. coli strain expresses huge amounts of cytosolic disulfide isomerase cytosolic and thus elevates the chance of disulfide formation for recombinant proteins. To improve the quality of proteins, furthermore, we lowered the expression temperatures to 16 °C.
- Cloning the sequences relevant for metal binding into the pASK plasmid
- Induction of protein expression under adapted conditions.
- Lysis of bacteria cells and protein precipitation by TCA.
- Preparation of protein samples and analysis by SDS-PAGE (VERWEIS).
- Transfer of separated proteins onto a PVDF membrane and an immunostaining(VERWEIS)by an anti-6xHistidine-tag antibody.
Labwork 2
Results