共 44 条
Design of Peptide Inhibitors for the Importin α/β Nuclear Import Pathway by Activity-Based Profiling
被引:181
作者:

Kosugi, Shunichi
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机构:
Keio Univ, Inst Adv Biosci, Tsuruoka, Yamagata 9970017, Japan
Keio Univ, Fac Sci & Technol, Dept Biosci & Informat, Yokohama, Kanagawa 2238522, Japan
Nara Inst Sci & Technol, Grad Sch Biol Sci, Ikoma 6300192, Japan Keio Univ, Inst Adv Biosci, Tsuruoka, Yamagata 9970017, Japan

Hasebe, Masako
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h-index: 0
机构:
Keio Univ, Inst Adv Biosci, Tsuruoka, Yamagata 9970017, Japan Keio Univ, Inst Adv Biosci, Tsuruoka, Yamagata 9970017, Japan

Entani, Tetsuyuki
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h-index: 0
机构:
Nara Inst Sci & Technol, Grad Sch Biol Sci, Ikoma 6300192, Japan Keio Univ, Inst Adv Biosci, Tsuruoka, Yamagata 9970017, Japan

Takayama, Seiji
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h-index: 0
机构:
Nara Inst Sci & Technol, Grad Sch Biol Sci, Ikoma 6300192, Japan Keio Univ, Inst Adv Biosci, Tsuruoka, Yamagata 9970017, Japan

Tomita, Masaru
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机构:
Keio Univ, Inst Adv Biosci, Tsuruoka, Yamagata 9970017, Japan Keio Univ, Inst Adv Biosci, Tsuruoka, Yamagata 9970017, Japan

Yanagawa, Hiroshi
论文数: 0 引用数: 0
h-index: 0
机构:
Keio Univ, Inst Adv Biosci, Tsuruoka, Yamagata 9970017, Japan
Keio Univ, Fac Sci & Technol, Dept Biosci & Informat, Yokohama, Kanagawa 2238522, Japan Keio Univ, Inst Adv Biosci, Tsuruoka, Yamagata 9970017, Japan
机构:
[1] Keio Univ, Inst Adv Biosci, Tsuruoka, Yamagata 9970017, Japan
[2] Keio Univ, Fac Sci & Technol, Dept Biosci & Informat, Yokohama, Kanagawa 2238522, Japan
[3] Nara Inst Sci & Technol, Grad Sch Biol Sci, Ikoma 6300192, Japan
来源:
CHEMISTRY & BIOLOGY
|
2008年
/
15卷
/
09期
关键词:
D O I:
10.1016/j.chembiol.2008.07.019
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:
Despite the current availability of selective inhibitors for the classical nuclear export pathway, no inhibitor for the classical nuclear import pathway has been developed. Here we describe the development of specific inhibitors for the importin alpha/beta pathway using a novel method of peptide inhibitor design. An activity-based profile was created via systematic mutational analysis of a peptide template of a nuclear localization signal. An additivity-based design using the activity-based profile generated two peptides with affinities for importin alpha that were approximately 5 million times higher than that of the starting template sequence. The high affinity of these peptides resulted in specific inhibition of the importin alpha/beta pathway. These peptide inhibitors provide a useful tool for studying nuclear import events. Moreover, our inhibitor design method should enable the development of potent inhibitors from a peptide seed.
引用
收藏
页码:940 / 949
页数:10
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