Biomod/2013/StJohns/results: Difference between revisions

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*[[Biomod/2013/StJohns/results#Claw Visualization|We have visualized the above versions of the claw on AFM to show that they take the predicted shape.]]
*[[Biomod/2013/StJohns/results#Claw Visualization|We have visualized the above versions of the claw on AFM to show that they take the predicted shape.]]
*We have shown that the above versions of the claw form tight bands on a gel, indicating a single primary product of the anneal.
*We have shown that the above versions of the claw form tight bands on a gel, indicating a single primary product of the anneal.
*We have verified that FRET-tagged origami can be visualized in a gel, providing easy visual discrimination between differently-tagged versions of the claw.
*[[Biomod/2013/StJohns/results#Claw Visualization|We have verified that FRET-tagged origami can be visualized in a gel, providing easy visual discrimination between differently-tagged versions of the claw.]]
*[[Biomod/2013/StJohns/results#Claw Visualization|We have demonstrated a binding interaction between the functionalized claw and functionalized capsid as well as a lack of interaction between the nonfunctionalized claw and capsid.]]
*[[Biomod/2013/StJohns/results#Claw Visualization|We have demonstrated a binding interaction between the functionalized claw and functionalized capsid as well as a lack of interaction between the nonfunctionalized claw and capsid.]]
*We have not been able to differentiate bound and unbound complexes via DLS.
*We have not been able to differentiate bound and unbound complexes via DLS.

Revision as of 12:10, 24 October 2013

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For optimal viewing experience, please enlarge this window to at least 1024 pixels.

Summary

Data

Claw Visualization

Below are AFM images of the claws alone, with and without binding elements. <html><center><table><tbody align="center"><tr><td><img src="http://openwetware.org/images/thumb/6/66/Lukemanlab-Bluntclaw_afm.png/200px-Lukemanlab-Bluntclaw_afm.png"></td><td><img src="http://openwetware.org/images/thumb/9/9f/Lukemanlab-Stickyclaw_afm.png/200px-Lukemanlab-Stickyclaw_afm.png"></td></tr><tr><td>"Blunt" claw</td><td>"Sticky" claw</td></tr></tbody></table></center></html>

Binding Interaction

We used gel electrophoresis to characterize the binding interaction between origami structures and capsids with and without binding elements.

No binding between WT capsids and any DO,
‘sticky’ DO bind sticky capsids strongly;
however, blunt DO binds sticky capsids.

FRET

<html> <center> <table> <tbody align="center"> <tr> <td> <img src="http://openwetware.org/images/thumb/d/d5/1a_ch1_FRET.tif/345px-1a_ch1_FRET.tif.png"> </td> <td> <img src="http://openwetware.org/images/thumb/6/69/1a_ch2_DONOR.tif/345px-1a_ch2_DONOR.tif.png"> </td> <td> <img src="http://openwetware.org/images/thumb/c/ce/1a_ch3_ACCEPTOR.tif/345px-1a_ch3_ACCEPTOR.tif.png"> </td> </tr> <tr> <td>FRET</td><td>DONOR</td><td>ACCEPTOR</td> </tr> </tbody> </table> </center> </html>


To determine FRET, FRET intensity - DONOR intensity - ACCEPTOR intensity DA(i,j) = DA(i,j) - beta_leak * DD(i,j) - beta_dir * AA (i,j)