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. 2013 Apr;33(8):1528–1545. doi: 10.1128/MCB.01442-12

Fig 3.

Fig 3

Analysis using plusTipTracker. (A) Work flow of ex vivo assay evaluating the effect of candidate CLASP-interacting proteins on MT dynamics. (B) (i) Cells expressing EB1-GFP selectively mark the plus end of growing MT forming an EB1 comet. (ii) Comet detection identifies EB1-GFP-positive MT ends. (iii) MT growth subtracks are reconstructed using a single-particle-tracking algorithm, followed by linkage of detected comets with a high probability for correspondence between consecutive frames. Velocity, lifetime, and displacement of each MT growth subtrack are extracted. (C) Growth subtracks color coded by average frame-to-frame velocity for a small population of control (i) and CLASP dsRNA-treated (ii) cells. CLASP knockdown results in higher average growth subtrack velocities compared to that for the control. Bars = 10 μm.