Fig. 7. RanGDP removes higher amounts of importin-ß from extracts of
KetelD eggs than from extracts of wild-type (WT) eggs.
RanQ69L protein binds higher amounts of importin-ß protein from WT egg
extract than from extract of KetelD eggs. GST protein was
used as a negative control (A, left). RanQ69L protein removes high amounts of
purified WT importin-ß but not purified P446L mutant protein. At the same
time RanGDP removes higher amounts of purified P446L importin-ß compared
with the purified WT importin-ß (A, right). More Ran is precipitated with
the anti-Ketel antibody from extracts of the KetelD eggs
than from extracts of WT eggs. (B, left). However, if an energy-regenerating
system and 3 µM (10 times the endogenous importin-ß concentration in
the extract) purified wild-type or P446L mutant importin-ß are added to
WT egg extract, more Ran is precipitated from the extract supplemented with WT
importin-ß (B, right). Wild-type importin-ß inhibits both exchange
of the labeled GTP from Ran (C) and GTP hydrolysis (D), whereas P446L mutant
importin-ß has no effect on both nucleotide exchange and GTP hydrolysis.
In C, the time course of nucleotide exchange is shown on a semi-logarithmic
scale and D shows the results of the reactions performed in duplicate.