Difference between revisions of "IGEM:Harvard/2006/Adaptamers/Notebook/2006-8-28"

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(Strand Displacement round 2)
 
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[[Image:cst828-displace5washesgraph.jpg]]
 
[[Image:cst828-displace5washesgraph.jpg]]
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This data confirmed much of what was seen for the same experiment on 8-26. while strand displacement successfully quenches adaptamer function, increasing amounts of displacement strand led to increased fluorescence. Most interestingly, samples containing displacement strands retained fluorescence following numerous washes in comparison to samples of only adaptamers. I have proposed a mechanism explaining this observation as follows:
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===Lever mechanism===
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Thrombin is represented by a rectangle, streptavidin by an oval. The double-helix regions of our adaptamers in effect create long, rigid rods (A). The longer these rods are, the more susceptible they are to washes since applying pressure toward the thrombin side of the adaptamer (see arrow in A) results in a large amount of mechanical advantage that enables the dissociation of the adaptamer from the surface of the streptavidin bead. This explains the lack of fluorescence observed using the adaptamer with the longest linking region, A50, despite Western Blot results. In contrast, addition of displacement strand (red) reduces the length of any rigid regions, bringing about flexibility that makes it less susceptible to washes (B). Moreover, displacement strands provide multiple attachment sites for T20, increasing the possibility of attaching multiple thrombins to a single streptavidin molecule.
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[[Image:LeverMechanism.jpg]]

Latest revision as of 18:23, 29 October 2006

8/28

Strand Displacement round 2

General setup = 40 pmol A20 + 100 uL Streptavidin magnetic beads + 160 pmol thrombin


Well Condition
1 general setup
2 general setup
3 adaptamer = A50
4 10 pmol R20.20 added
5 20 pmol R20.20 added
6 40 pmol R20.20 added
7 10 pmol R20.35 added
8 20 pmol R20.35 added
9 40 pmol R20.35 added
10 40 pmol T20 instead of A20
11 40 pmol S20 instead of A20
12 no thrombin added
  • After 3 washes

Image taken at intensity 3

Cst828-displace3washes.jpg

Cst828-displace3washesgraph.jpg

  • After 5 washes

Cst828-displace5washes.jpg

Cst828-displace5washesgraph.jpg


This data confirmed much of what was seen for the same experiment on 8-26. while strand displacement successfully quenches adaptamer function, increasing amounts of displacement strand led to increased fluorescence. Most interestingly, samples containing displacement strands retained fluorescence following numerous washes in comparison to samples of only adaptamers. I have proposed a mechanism explaining this observation as follows:

Lever mechanism

Thrombin is represented by a rectangle, streptavidin by an oval. The double-helix regions of our adaptamers in effect create long, rigid rods (A). The longer these rods are, the more susceptible they are to washes since applying pressure toward the thrombin side of the adaptamer (see arrow in A) results in a large amount of mechanical advantage that enables the dissociation of the adaptamer from the surface of the streptavidin bead. This explains the lack of fluorescence observed using the adaptamer with the longest linking region, A50, despite Western Blot results. In contrast, addition of displacement strand (red) reduces the length of any rigid regions, bringing about flexibility that makes it less susceptible to washes (B). Moreover, displacement strands provide multiple attachment sites for T20, increasing the possibility of attaching multiple thrombins to a single streptavidin molecule.

LeverMechanism.jpg