Biomod/2013/StJohns/results

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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

Below is a gel demonstrating that versions of the claw tagged with different fluorescent elements can be visually distinguished on a gel.

Each different color band corresponds to a different fluorescent tag.
The six bands on the left are 'blunt' claw and the six on the right are 'sticky' claw.
Odd-numbered lanes contain 0.1 pmol claw, while even-numbered lanes contain 0.2 pmol.

DLS

Our DLS measurements confirmed that the origami control structure and the capsid were of different sizes. However, when performing DLS on a mix of nonfunctionalized origami and capsid, we found only a single peak rather than peaks showing two differently-sized objects. Based on data from other experiments, it is unlikely that this represents a binding interaction. We are currently investigating the source of this anomaly. [[Image:Lukemanlab-2013-0003.png|thumb|400px|center]