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Fig. 3. Binding of tau to individual MTs depends on MT curvature. (A) Fluorescence micrograph of a fibroblast expressing GFP-tau. Individual MTs can be detected at the lamella region. The boxed regions are shown below at a higher magnification. (B-D) A series of fluorescence images of the lamella of the fibroblast. Images were taken at 3-second intervals. Sites of higher MT curvature (arrows) display higher levels of fluorescence intensity. (E) Fluorescence micrograph of the axonal shaft with a flat growth cone-like protrusion at the lateral edge. The boxed region of the image on the left is shown at higher magnification on the right as a series of images acquired at 3-second intervals. (F) Quantitative analysis of the data for GFP-tau-labeled MTs in fibroblasts (open triangles), GFP-tau-labeled MTs in neurons (stars), and GFP-tubulin-decorated MTs in fibroblasts (filled triangles). Each datum point represents background-subtracted fluorescence intensity of MT at the site of high curvature (I) normalized to that at the straight segment of the same MT (Io), versus the radius of MT curvature (RMT). Data for the cells expressing GFP-tau are grouped together and fitted with a single exponential.





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