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. 2014 Mar;34(6):965–977. doi: 10.1128/MCB.01605-13

FIG 4.

FIG 4

Single particle tracking (SPT) detects short-lived erbB2-erbB3 heterodimers and longer-lived erbB3 homodimers. (A and B) Receptor dimerization behavior based on tracking of a pair of QD-tagged receptors over time. Shown are representative plots of separation distances for an erbB2-erbB3 heterodimer on CHO cells expressing exogenous HA-erbB2 and untagged erbB3 (A) and endogenous erbB3 receptors interacting on SKBR3 cells (B). Horizontal lines indicate state calls (right axis, dimer, coconfined, or separated receptors) as determined by a Viterbi algorithm. Insets show images of pairs at specific time frames. Scale bar, 1 μm. (C) Diagram illustrating interaction states of erbB3 tracked with two colors of QD-HRG and with different levels of unlabeled erbB2 (gray spheres). (D to I) Histograms plotting the distribution of dimer lifetimes for receptor pairs as indicated (diagrams). koff values are predicted from the HMM analysis.