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Nucleic Acids Research 2005 33(22):e190; doi:10.1093/nar/gni188
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Published online 13 December 2005

© The Author 2005. Published by Oxford University Press. All rights reserved
The online version of this article has been published under an open access model. Users are entitled to use, reproduce, disseminate, or display the open access version of this article for non-commercial purposes provided that: the original authorship is properly and fully attributed; the Journal and Oxford University Press are attributed as the original place of publication with the correct citation details given; if an article is subsequently reproduced or disseminated not in its entirety but only in part or as a derivative work this must be clearly indicated. For commercial re-use, please contact journals.permissions{at}oxfordjournals.org


Methods Online

Quantum dots to monitor RNAi delivery and improve gene silencing

Alice A. Chen1, Austin M. Derfus2, Salman R. Khetani1,2 and Sangeeta N. Bhatia1,2,3,*

1Harvard-M.I.T. Division of Health Sciences and Technology/Electrical Engineering and Computer Science, Massachusetts Institute of Technology MA, USA 2Department of Bioengineering, University of California at San Diego CA, USA 3Division of Medicine, Brigham & Women's Hospital Boston, MA, USA

*To whom correspondence should be addressed at Laboratory for Multiscale Regenerative Technologies, 77 Massachusetts Avenue, E19-502D, Cambridge, MA 02139, USA. Tel: +617 324 0221; Fax: +617 324 0740; Email: sbhatia{at}mit.edu

Received May 24, 2005. Revised November 22, 2005. Accepted November 22, 2005.

A critical issue in using RNA interference for identifying genotype/phenotype correlations is the uniformity of gene silencing within a cell population. Variations in transfection efficiency, delivery-induced cytotoxicity and ‘off target’ effects at high siRNA concentrations can confound the interpretation of functional studies. To address this problem, we have developed a novel method of monitoring siRNA delivery that combines unmodified siRNA with seminconductor quantum dots (QDs) as multi color biological probes. We co-transfected siRNA with QDs using standard transfection techniques, thereby leveraging the photostable fluorescent nanoparticles to track delivery of nucleic acid, sort cells by degree of transfection and purify homogenously-silenced subpopulations. Compared to alternative RNAi tracking methods (co-delivery of reporter plasmids and end-labeling the siRNA), QDs exhibit superior photostability and tunable optical properties for an extensive selection of non-overlapping colors. Thus this simple, modular system can be extended toward multiplexed gene knockdown studies, as demonstrated in a two color proof-of-principle study with two biological targets. When the method was applied to investigate the functional role of T-cadherin (T-cad) in cell–cell communication, a subpopulation of highly silenced cells obtained by QD labeling was required to observe significant downstream effects of gene knockdown.


The authors wish it be known that, in their opinion, the first two authors should be regarded as joint First Authors


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W.-l. Liu, M. Stevenson, L. W. Seymour, and K. D. Fisher
Quantification of siRNA using competitive qPCR
Nucleic Acids Res., January 1, 2009; 37(1): e4 - e4.
[Abstract] [Full Text] [PDF]



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