Activation of different split functionalities on re-association of RNA-DNA hybrids

被引:0
作者
Afonin, Kirill A. [1 ]
Viard, Mathias [1 ,2 ]
Martins, Angelica N. [3 ]
Lockett, Stephen J. [4 ]
Maciag, Anna E. [2 ,5 ]
Freed, Eric O. [3 ]
Heldman, Eliahu [2 ,6 ]
Jaeger, Luc [7 ]
Blumenthal, Robert [1 ]
Shapiro, Bruce A. [1 ]
机构
[1] NCI, Ctr Canc Res, Nanobiol Program, Frederick, MD 21702 USA
[2] NCI, Basic Sci Program, SAIC Frederick, Frederick Natl Lab Canc Res, Frederick, MD 21702 USA
[3] NCI, HIV Drug Resistance Program, Frederick, MD 21702 USA
[4] NCI, Adv Technol Program, SAIC Frederick, Frederick Natl Lab Canc Res, Frederick, MD 21702 USA
[5] NCI, Biol Chem Lab, Frederick, MD 21702 USA
[6] Ben Gurion Univ Negev, IL-84105 Beer Sheva, Israel
[7] Univ Calif Santa Barbara, Dept Chem & Biochem, Biomol Sci & Engn Program, Santa Barbara, CA 93106 USA
关键词
EMERGING FIELD; SIRNA; NANOPARTICLES; DICER; DELIVERY; HYBRIDIZATION; INTERFERENCE; REQUIREMENT; ANATOMY; HUMANS;
D O I
10.1038/NNANO.2013.44
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Split-protein systems, an approach that relies on fragmentation of proteins with their further conditional re-association to form functional complexes, are increasingly used for various biomedical applications. This approach offers tight control of protein functions and improved detection sensitivity. Here we report a similar technique based on a pair of RNA-DNA hybrids that can be used generally for triggering different split functionalities. Individually, each hybrid is inactive but when two cognate hybrids re-associate, different functionalities are triggered inside mammalian cells. As a proof of concept, this work mainly focuses on the activation of RNA interference. However, the release of other functionalities (such as resonance energy transfer and RNA aptamer) is also shown. Furthermore, in vivo studies demonstrate a significant uptake of the hybrids by tumours together with specific gene silencing. This split-functionality approach presents a new route in the development of 'smart' nucleic acid-based nanoparticles and switches for various biomedical applications.
引用
收藏
页码:296 / 304
页数:9
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