Interaction between NTF2 and xFxFG-containing nucleoporins is required to mediate nuclear import of RanGDP

被引:151
作者
Bayliss, R
Ribbeck, K
Akin, D
Kent, HM
Feldherr, CM
Görlich, D
Stewart, M
机构
[1] MRC, Mol Biol Lab, Cambridge CB2 2QH, England
[2] Heidelberg Univ, Zentrum Mol Biol, D-69120 Heidelberg, Germany
[3] Univ Florida, Coll Med, Dept Anat & Cell Biol, Gainesville, FL 32610 USA
基金
美国国家科学基金会;
关键词
nuclear trafficking; nucleoporins; transport;
D O I
10.1006/jmbi.1999.3166
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nuclear transport factor (NTF2) is a small, homodimeric protein that binds to both RanGDP and xFxFG repeat-containing nucleoporins, such as yeast Nsp1p and vertebrate p62. NTF2 is required for efficient nuclear protein import and has been shown to mediate the nuclear import of RanGDP. We have used the-crystal structures of rat NTF2 and its complex with RanGDP to design:a mutant, W7A-NTF2, in which the affinity for xFxFG-repeat nucleoporins is reduced while wild-type binding to RanGDP is retained. The 2.5 Angstrom resolution crystal structure of W7A-NTF2 is virtually superimposable upon the wild-type protein structure, indicating that the mutation had not introduced a more general conformational change. Therefore, our data suggest that the exposed side-chain of residue 7 is crucial to the interaction between NTF2 and xFxFG repeat-containing nucleoporins. Consistent-with its reduced affinity for xFxFG nucleoporins, fluorescently labelled W7A-NTF2 binds less strongly to the nuclear envelope of permeabilized cultured cells than wild-type NTF2 and, when microinjected into Xenopus oocytes, colloidal gold coated with W7A-NTF2 binds less strongly to the central channel of nuclear pore complexes than wild-type NTF2-coated gold. Significantly, W7A-NTF2 only weakly stimulated the nuclear import of fluorescein-labelled RanGDP, providing direct evidence that an interaction between NTF2 and xFxFG repeat-containing nucleoporins is required to mediate the nuclear import of RanGDP. (C) 1999 Academic Press.
引用
收藏
页码:579 / 593
页数:15
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