spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    


Right arrow Help viewing high resolution images
Right arrow Return to article
(Downloading may take up to 30 seconds.
If the slide opens in your browser, select File -> Save As to save it.)

Click on image to view larger version.


Figure 4


Fig. 4. A PtdIns(3)P probe is redirected from EEA1-positive regions into Hrs-containing microdomains through clathrin binding. (A) Schematic representation of the 2xFYVE-Hrs CT chimeric constructs, with and without the clathrin-box motif. HeLa cells were transiently co-transfected with Rab5Q79L and (B) myc-2xFYVE-Hrs CT or (D) myc-2xFYVE-Hrs CT{Delta}CB, and stained with anti-myc and anti-EEA1 antibodies for immunofluorescence confocal microscopy. Alternatively, cells were triple transfected with Rab5Q79L and (C) myc-2xFYVE-Hrs CT and YFP-Hrs or (E) myc-2xFYVE-Hrs CT{Delta}CB and YFP-Hrs, and stained with anti-myc antibodies. Insets show two different enlarged endosomes from each transfection. Yellow indicates colocalisation. Bar, 5 µm. The level of colocalisation of the different proteins on endosome membranes was quantified as described in Materials and Methods (F). Error bars give the mean + s.e.m. myc-2xFYVE-Hrs CT + EEA1, n=19; myc-2xFYVE-Hrs CT + YFP-Hrs, n=27; myc-2xFYVE-Hrs CT{Delta}CB + EEA1, n=27; 2xFYVE-Hrs CT{Delta}CB + YFP-Hrs, n=29.





Right arrow Return to article