Team:Penn/Targeting

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To verify that our SKBR3 cells overexpressed HER2, we immunostained for HER2 (primary anti-Neu Mouse Igg, Santa Cruz Biotechnology and secondary donkey anti-mouse Alexa-Fluor 647 conjugate, Jackson Immunoresearch) and visualized the cells on a confocal microscope. As expected, HER2 was overexpressed in SKBR3 cells (Figure 10).</p>
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To verify that our SKBR3 cells overexpressed HER2, we immunostained for HER2 (primary anti-Neu Mouse Igg, Santa Cruz Biotechnology and secondary donkey anti-mouse Alexa-Fluor 647 conjugate, Jackson Immunoresearch) and visualized the cells on a confocal microscope. As expected, HER2 was overexpressed in SKBR3 cells (Figure 1).</p>
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<div class="fignew"><div align="center"><img src="https://static.igem.org/mediawiki/2012/e/e0/SKBR3_%28%2BDAPI%29_%28%2BAB1%29_%28%2BAB2%29_630x.jpg" height="400"><br>
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<div class="fignew"><div align="center"><img src="https://static.igem.org/mediawiki/2012/e/e0/SKBR3_%28%2BDAPI%29_%28%2BAB1%29_%28%2BAB2%29_630x.jpg" height="400" width="400"><br>
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<b>Figure 10</b></div>Figure 10: SKBR3 cells over-express HER2 on their surface. Red indicates HER2 (Alexa-Fluor 647), Blue indicates DAPI.</div>
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<b>Figure 1</b></div>Figure 1: SKBR3 cells over-express HER2 on their surface. Red indicates HER2 (Alexa-Fluor 647), Blue indicates DAPI.</div>
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<div class="fignew"><div align="center"><img src="https://static.igem.org/mediawiki/2012/7/7a/HER2-Breast-Tissue.jpg" height="400"/><br>
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<div class="fignew"><div align="center"><img src="https://static.igem.org/mediawiki/2012/7/7a/HER2-Breast-Tissue.jpg" height="400" width="400"><br>
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<b>Figure 11</b></div>Figure 11: Images of breast cancer cells removed from human tissue reveal similar HER 2 expression to results obtained in Figure 10.  </div></div>
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<b>Figure 2</b></div>Figure 2: Images of breast cancer cells removed from human tissue reveal similar HER 2 expression to results obtained in Figure 2.  </div></div>
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<p style="color:black;text-indent:30px;">To assay whether our DARPin-displaying E. coli bound to SKBR3 cells preferentially, we conducted experiments in which our bacteria were co-incubated with SKBR3 or HEK293T cells. The DARPin-displaying bacteria were co-transformed with eGFP for easy visualization. These experiments are still in progress to optimize the co-incubation and gentamycin protection protocol (we designed this type of experiment ourselves since it has not been done before). However, preliminary results are exciting and show preferential binding to SKBR3 cells (Figure 12).</p>
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<p style="color:black;text-indent:30px;">To assay whether our DARPin-displaying E. coli bound to SKBR3 cells preferentially, we conducted experiments in which our bacteria were co-incubated with SKBR3 or HEK293T cells. The DARPin-displaying bacteria were co-transformed with constitutively expressed eGFP (pACBB-eGFP plasmid) for easy visualization. The goal was to show SKBR3-specific binding of eGFP labeled bacteria, and only when they were induced with IPTG to produce INPNC-DARPin. Preliminary results are exciting and show preferential binding to SKBR3 cells. In culture plates with low-HER2 HEK293T cells, no green bacteria were observed bound to the cells. IPTG-induced bacteria bound selectively to SKBR3 cells and we visualized this binding by confocal microscopy (Figure 3).</p>
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<div class="fig11"><b>Figure 12</b>: SKBR3 cells overexpress HER2 and DARPin-displaying bacteria bind to their surface. Red indicates HER2 (Alexa-Fluor 647), Blue indicates DAPI. Green indicates eGFP. Bacteria were co-incubated at a Multiplicity of Infection of 200:1 and washed three times after co-incubation followed by a 50ug/mL gentamicin protection assay.</p></div>
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<div class="fig11"><b>Figure 3</b>: SKBR3 cells overexpress HER2 and DARPin-displaying bacteria bind to their surface. Red indicates HER2 (Alexa-Fluor 647). Blue indicates DAPI. Green indicates eGFP. Bacteria were co-incubated at a Multiplicity of Infection of 200:1 and washed three times after co-incubation followed by a 50ug/mL gentamicin protection assay.</p></div>
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Taking a closer look at the SKBR3 + Induced Bacteria group, one can observe our eGFP labeled bacteria bound directly to the HER2 on SKBR3 cells (Figure 4)
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<div class="fig11"><b>Figure 4</b>: Direct binding of INPNC-DARPin expressing, eGFP-labeled bacteria to SKBR3 cells.</p></div>
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In summary, we demonstrated surface display of DARPin H10-2-G3 for the first time and have preliminary evidence showing our DARPin-displaying bacteria can target cancer cells. We also developed a generalized surface display BioBrick for any iGEM team to use.<br /> </div></div>
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<b>Conclusion</b>
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In summary, we demonstrated surface display of DARPin H10-2-G3 for the first time and have demonstrated that our DARPin-displaying bacteria can target cancer cells <i>in vitro</i>. We also developed a generalized surface display BioBrick for any iGEM team to use.<br /> </div></div>
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Latest revision as of 02:59, 27 October 2012

Penn 2012 iGEM Wiki

Image Map

Testing the Displayed HER2 DARPin on Cancer Cells

After verifying that the DARPin was displayed on the cell surface, we sought to test whether it could allow binding to HER2-overexpressing cancer cells. We were generously provided SKBR3 cells by the lab of Matthew Lazzara. These cells are derived from breast cancer cells and over-express HER2. We also obtained Human Embryonic Kidney (HEK) 293T cells, which express a low amount of HER2, to act as controls.

To verify that our SKBR3 cells overexpressed HER2, we immunostained for HER2 (primary anti-Neu Mouse Igg, Santa Cruz Biotechnology and secondary donkey anti-mouse Alexa-Fluor 647 conjugate, Jackson Immunoresearch) and visualized the cells on a confocal microscope. As expected, HER2 was overexpressed in SKBR3 cells (Figure 1).


Figure 1
Figure 1: SKBR3 cells over-express HER2 on their surface. Red indicates HER2 (Alexa-Fluor 647), Blue indicates DAPI.

Figure 2
Figure 2: Images of breast cancer cells removed from human tissue reveal similar HER 2 expression to results obtained in Figure 2.

To assay whether our DARPin-displaying E. coli bound to SKBR3 cells preferentially, we conducted experiments in which our bacteria were co-incubated with SKBR3 or HEK293T cells. The DARPin-displaying bacteria were co-transformed with constitutively expressed eGFP (pACBB-eGFP plasmid) for easy visualization. The goal was to show SKBR3-specific binding of eGFP labeled bacteria, and only when they were induced with IPTG to produce INPNC-DARPin. Preliminary results are exciting and show preferential binding to SKBR3 cells. In culture plates with low-HER2 HEK293T cells, no green bacteria were observed bound to the cells. IPTG-induced bacteria bound selectively to SKBR3 cells and we visualized this binding by confocal microscopy (Figure 3).

Figure 3: SKBR3 cells overexpress HER2 and DARPin-displaying bacteria bind to their surface. Red indicates HER2 (Alexa-Fluor 647). Blue indicates DAPI. Green indicates eGFP. Bacteria were co-incubated at a Multiplicity of Infection of 200:1 and washed three times after co-incubation followed by a 50ug/mL gentamicin protection assay.



Taking a closer look at the SKBR3 + Induced Bacteria group, one can observe our eGFP labeled bacteria bound directly to the HER2 on SKBR3 cells (Figure 4)

Figure 4: Direct binding of INPNC-DARPin expressing, eGFP-labeled bacteria to SKBR3 cells.



Conclusion

In summary, we demonstrated surface display of DARPin H10-2-G3 for the first time and have demonstrated that our DARPin-displaying bacteria can target cancer cells in vitro. We also developed a generalized surface display BioBrick for any iGEM team to use.

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