Anchor Binding Capacity

What you will need:

• Paramagnetic Streptavidin Beads
• Annealed Anchor

Binding Capacity

• Prepare a 20 μM solution of the Anchor (same as but using 30 μL water instead of 80 μL)
• Set up a set of microcentrifuge tubes with 10, 20, 30, 40, 50, 60, 70, 80 μL of 4 mg mL^-1 beads dispensed into the respectively labelled tubes.
• Wash the beads twice with 100 μL Wash/Binding buffer and once with 100 μL water, then aspirate water off the beads.
• Prepare 4 μL of the 20 μM Anchor solution to separate tubes (corresponding to which bead-containing tube they will be added to) along with enough water to bring the final solution volume up to half the dispensed bead volume. (i.e. to the 40 μL tube add 4 μL Anchor + 16 μL water).
• Add half of this solution to the tubes containing the washed beads. Retain the other half.
• Suspend the beads in the DNA solution.
• Let bind at room temperature for 10 minutes.
• Pellet the beads with a magnet and aspirate the solution.
• Take readings at A₂₆₀ with a UV-Vis Spectrophotometer of the DNA solutions prior to binding to bead (the half you retained) and after binding to bead (the aspirated solution). (ng of DNA can also be found by in-gel band intensity quantification methods)

By doing the binding capacity in this manner we found that binding capacity is highly dependant on DNA and bead concentration (see the graphs "here"). Thus, we simply used the calculated binding capacity for 40 μL of beads since this is the volume we use for all builds. A better binding capacity assay should be developed, but due to time constraints this method proved good enough since multiple runs of this experiment yielded numbers with small standard deviation:
209 +/- 20 pmol mg^-1