F. Tebar et al., EPS15 IS A COMPONENT OF CLATHRIN-COATED PITS AND VESICLES AND IS LOCATED AT THE RIM OF COATED PITS, The Journal of biological chemistry, 271(46), 1996, pp. 28727-28730
Eps15, a phosphorylation substrate of the epidermal growth factor (EGF
) receptor kinase, has been shown to bind to the alpha-subunit of the
clathrin-associated protein complex AP-2. Here we report that in cells
, virtually all Eps15 interacts with the cytosol and membrane-bound fo
rms of AP-2. This association is not affected by the treatment of cell
s with EGF. Immunofluorescence microscopy reveals nearly absolute co-l
ocalization of Eps15 with AP-2 and clathrin, and analysis by immunoele
ctron microscopy shows that the localization of membrane-associated Ep
s15 is restricted to the profiles corresponding to endocytic coated pi
ts and vesicles. Unexpectedly, Eps15 was found at the edge of forming
coated pits and at the rim of budding coated vesicles. This asymmetric
distribution is in sharp contrast to the localization of AP-2 that sh
ows an even distribution along the same types of clathrin-coated struc
tures. These findings suggest several possible regulatory roles of Eps
15 during the formation of coated pits.