Aptamers that bind specifically to human KPNA2 (importin-α1) and efficiently interfere with nuclear transport

被引:7
|
作者
Yasuhara, Noriko [1 ,3 ]
Kumar, Penmetcha K. R. [2 ]
机构
[1] Natl Inst Biomed Innovat Hlth & Nutr, Lab Nucl Transport Dynam, 7-6-8 Sito Asagi, Ibaraki, Osaka 5670085, Japan
[2] Natl Inst Adv Ind Sci & Technol, Biomed Res Inst, Cent 6,1-1-1 Higashi, Tsukuba, Ibaraki 3058566, Japan
[3] Nihon Univ, Dept Life Sci, Coll Humanities & Sci, Setagaya Ku, 3-25-40 Sakurajousui, Tokyo 1568550, Japan
关键词
Aptamer; Cancer; importin-alpha; nuclear transport; RNA; INFLUENZA-VIRUSES; PROTEIN IMPORT; RNA APTAMER; ALPHA; LOCALIZATION; CELLS; HEMAGGLUTININ; MEMBRANE; CANCER; TRANSLOCATION;
D O I
10.1093/jb/mvw032
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
The importin-alpha family of proteins plays an important role in the eukaryotic importin/exportin nuclear transport system. These proteins recognize a nuclear localization signal (NLS) within cargo proteins and import them into the nucleus through nuclear pores, in a process mediated by importin-beta. Recent studies have shown that importin-alpha proteins specifically recognize the NLS of several cellular factors and viral proteins, thus regulating their movement. Dysregulation of importin-alpha is a common hallmark of many pathologies including, multiple cancers. In this study, we isolated aptamers 76 and 72, which bind specifically and efficiently to KPNA2, a member of a subfamily of importin-alpha 1. Both of these aptamers bind to KPNA2 with an equilibrium dissociation constant (Kd) of 150nM and discriminate between KPNA2 and other sub-family members of importin-alpha, such as KPNA1 and KPNA3. These aptamers specifically interfere with the nuclear transport of cargo proteins mediated by KPNA2 but neither with KPNA1 nor KPNA3, which belongs to other subfamily of importins. These results suggest that the selected aptamers (76 and 72) warrant further study to explore not only their application in cancer diagnosis but also their use as a specific reagent to potentially block KPNA2-dependent nuclear transport of macromolecules across the nuclear membrane.
引用
收藏
页码:259 / 268
页数:10
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