scholarly journals NLS Peptide Conjugated Molecular Beacons for Visualizing Nuclear RNA in Living Cells

2008 ◽  
Vol 19 (11) ◽  
pp. 2205-2211 ◽  
Author(s):  
Nitin Nitin ◽  
Gang Bao
Lab on a Chip ◽  
2011 ◽  
Vol 11 (22) ◽  
pp. 3908 ◽  
Author(s):  
Jennifer Claire Alexander ◽  
Abhay Pandit ◽  
Gang Bao ◽  
David Connolly ◽  
Yury Rochev

Author(s):  
Andrew Tsurkas ◽  
Gang Bao

Real-time imaging of gene expression in living cells has the potential to significantly impact clinical and laboratory studies of cancer, including cancer diagnosis and analysis. Molecular beacons (MBs) provide a simple and promising tool for the detection of target mRNA as tumor markers due to their high signal-to-background ratio, and their improved specificity in detecting point mutations. However, the harsh intracellular environment does limit the sensitivity of MB-based gene detection. Specifically, MBs bound to target mRNAs cannot be distinguished from those degraded by nucleases, or opened due to non-specific interactions. To overcome this difficulty, we have developed a novel dual FRET molecular beacons approach in which a pair of molecular beacons, one with a donor fluorophore and a second with an acceptor fluorophore, hybridize to adjacent regions on the same target resulting in fluorescence resonance energy transfer (FRET). The detection of a FRET signal leads to a substantially increased signal-to-background ratio compared with that in single molecular beacon assays and enables discrimination between fluorescence due to specific probe/target hybridization and a variety of false-positive events. We have performed systematic in-solution and cellular studies of dual FRET molecular beacon and demonstrated that this new approach allows for real-time imaging of gene expression in living cells.


2012 ◽  
Vol 7 (9) ◽  
pp. 1586-1595 ◽  
Author(s):  
Irina E. Catrina ◽  
Salvatore A. E. Marras ◽  
Diana P. Bratu

2011 ◽  
Vol 2011 ◽  
pp. 1-15 ◽  
Author(s):  
Ricardo Monroy-Contreras ◽  
Luis Vaca

Recent advances in RNA functional studies highlights the pivotal role of these molecules in cell physiology. Diverse methods have been implemented to measure the expression levels of various RNA species, using either purified RNA or fixed cells. Despite the fact that fixed cells offer the possibility to observe the spatial distribution of RNA, assays with capability to real-time monitoring RNA transport into living cells are needed to further understand the role of RNA dynamics in cellular functions. Molecular beacons (MBs) are stem-loop hairpin-structured oligonucleotides equipped with a fluorescence quencher at one end and a fluorescent dye (also called reporter or fluorophore) at the opposite end. This structure permits that MB in the absence of their target complementary sequence do not fluoresce. Upon binding to targets, MBs emit fluorescence, due to the spatial separation of the quencher and the reporter. Molecular beacons are promising probes for the development of RNA imaging techniques; nevertheless much work remains to be done in order to obtain a robust technology for imaging various RNA molecules together in real time and in living cells. The present work concentrates on the different requirements needed to use successfully MB for cellular studies, summarizing recent advances in this area.


2009 ◽  
Vol 02 (04) ◽  
pp. 315-324 ◽  
Author(s):  
ANTONY K. CHEN ◽  
ANDREW TSOURKAS

There is a growing realization that cell-to-cell variations in gene expression have important biological consequences underlying phenotype diversity and cell fate. Although analytical tools for measuring gene expression, such as DNA microarrays, reverse-transcriptase PCR and in situ hybridization have been widely utilized to discover the role of genetic variations in governing cellular behavior, these methods are performed in cell lysates and/or on fixed cells, and therefore lack the ability to provide comprehensive spatial-dynamic information on gene expression. This has invoked the recent development of molecular imaging strategies capable of illuminating the distribution and dynamics of RNA molecules in living cells. In this review, we describe a class of molecular imaging probes known as molecular beacons (MBs), which have increasingly become the probe of choice for imaging RNA in living cells. In addition, we present the major challenges that can limit the ability of MBs to provide accurate measurements of RNA, and discuss efforts that have been made to overcome these challenges. It is envisioned that with continued refinement of the MB design, MBs will eventually become an indispensable tool for analyzing gene expression in biology and medicine.


2007 ◽  
Vol 35 (16) ◽  
pp. e105 ◽  
Author(s):  
Antony K. Chen ◽  
Mark A. Behlke ◽  
Andrew Tsourkas

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