Beilstein J. Nanotechnol.2016,7, 138–148, doi:10.3762/bjnano.7.16
here demonstrate that handles produced with our protein–DNA labelling procedure are excellent candidates for grasping single molecules exposing tags suitable for molecular recognition in time-critical molecular motor studies.
Keywords: DNA handles; optical tweezers; proteinlabels; single molecule
experiments for both proteinlabels. With DTT buffer the interaction rate was only 53% for neutravidin-DNA and 61% for streptavidin-DNA, and bead clusters were observed in 20–35% of the experiments. A nominal ratio of 40:1 enabled efficient single molecule force measurements (90%) with the complete protein
-labelled DNA construct against biotinylated beads (Figure 1a).
Rupture forces were analysed in all buffers for DHs with streptavidin or neutravidin labels, respectively. Rupture force distributions for both proteinlabels are shown in Figure 4. The rupture force distributions for both protein–DNA
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Figure 1:
Bead arrangements in different optical force measurements. a) PDHs tethered to an anti-DIG bead (2....