Journal Article

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

Noriko Yasuhara and Penmetcha K.R. Kumar

in The Journal of Biochemistry

Volume 160, issue 5, pages 259-268
Published in print November 2016 | ISSN: 0021-924X
Published online May 2016 | e-ISSN: 1756-2651 | DOI: https://dx.doi.org/10.1093/jb/mvw032
Aptamers that bind specifically to human KPNA2 (importin-α1) and efficiently interfere with nuclear transport

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The importin-α 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-β. Recent studies have shown that importin-α proteins specifically recognize the NLS of several cellular factors and viral proteins, thus regulating their movement. Dysregulation of importin-α 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-α1. Both of these aptamers bind to KPNA2 with an equilibrium dissociation constant (K d) of 150 nM and discriminate between KPNA2 and other sub-family members of importin-α, 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.

Keywords: Aptamer; Cancer; importin-α; nuclear transport; RNA

Journal Article.  5948 words.  Illustrated.

Subjects: Cell Biology ; Biotechnology ; Biochemistry ; Molecular and Cell Biology

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