Small molecule peptidomimetic inhibitors of importin α/β mediated nuclear transport

被引:25
作者
Ambrus, Geza [1 ]
Whitby, Landon R. [2 ]
Singer, Eric L. [1 ]
Trott, Oleg [3 ]
Choi, Euna [1 ]
Olson, Arthur J. [3 ]
Boger, Dale L. [2 ]
Gerace, Larry [1 ]
机构
[1] Scripps Res Inst, Dept Cell Biol, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA
[3] Scripps Res Inst, Dept Mol Biol, La Jolla, CA 92037 USA
关键词
High content screening; Nucleocytoplasmic transport; Importin beta; Small molecule inhibitor; Peptidomimetics; SOLUTION-PHASE STRATEGY; PROTEIN IMPORT; PORE COMPLEX; NUCLEOCYTOPLASMIC TRANSPORT; COMBINATORIAL LIBRARIES; CHEMICAL LIBRARIES; STRUCTURAL BASIS; LEPTOMYCIN-B; EXPORT; BETA;
D O I
10.1016/j.bmc.2010.08.038
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
Nucleocytoplasmic transport of macromolecules is a fundamental process of eukaryotic cells. Translocation of proteins and many RNAs between the nucleus and cytoplasm is carried out by shuttling receptors of the beta-karyopherin family, also called importins and exportins. Leptomycin B, a small molecule inhibitor of the exportin CRM1, has proved to be an invaluable tool for cell biologists, but up to now no small molecule inhibitors of nuclear import have been described. We devised a microtiter plate based permeabilized cell screen for small molecule inhibitors of the importin alpha/beta pathway. By analyzing peptidomimetic libraries, we identified beta-turn and alpha-helix peptidomimetic compounds that selectively inhibit nuclear import by importin alpha/beta but not by transportin. Structure-activity relationship analysis showed that large aromatic residues and/or a histidine side chain are required for effective import inhibition by these compounds. Our validated inhibitors can be useful for in vitro studies of nuclear import, and can also provide a framework for synthesis of higher potency nuclear import inhibitors. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:7611 / 7620
页数:10
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