Quantifying Gene Expression in Living Cells with Ratiometric Bimolecular Beacons.

Methods Mol Biol

Department of Biomedical Engineering, College of Engineering, Peking University, No. 5 Yiheyuan Road, Haidian District, Beijing, 100871, China.

Published: June 2018

Molecular beacons (MBs), a class of oligonucleotide-based probes, have enabled researchers to study various RNA molecules in their native live-cell contexts. However, it is also increasingly recognized that, when delivered into cells, MBs have the tendency to be sequestered into the nucleus where they may generate false positive signals. In an attempt to overcome this issue, MBs have been synthesized with chemically modified oligonucleotide backbones to confer greater biostability. Alternatively, strategies have been developed to minimize nuclear entry. In the latter approach, we have combined functional elements of MBs with functional elements of siRNAs that facilitate nuclear export to create a new RNA imaging platform called ratiometric bimolecular beacons (RBMBs). We showed that RBMBs exhibited long-term cytoplasmic retention, and hence a marginal level of false positive signals in living cells. Subsequent studies demonstrated that RBMBs could sensitively and accurately quantify mRNA transcripts engineered to contain multiple tandem repeats of an MB target sequence at the single-molecule level. In this chapter, we describe the synthesis of RBMBs and their applications for absolute quantification and tracking of single mRNA transcripts in cells.

Download full-text PDF

Source
http://dx.doi.org/10.1007/978-1-4939-7213-5_15DOI Listing

Publication Analysis

Top Keywords

living cells
8
ratiometric bimolecular
8
bimolecular beacons
8
false positive
8
positive signals
8
functional elements
8
mrna transcripts
8
quantifying gene
4
gene expression
4
expression living
4

Similar Publications

3D printing, as a layer-by-layer manufacturing technique, enables the customization of tissue engineering scaffolds. Surface modification of biomaterials is a beneficial approach to enhance the interaction with living cells and tissues. In this research, a polylactic acid/polyethylene glycol scaffold containing 30 % bredigite nanoparticles (PLA/PEG/B) was fabricated utilizing fused deposition modeling (FDM) 3D printing.

View Article and Find Full Text PDF

Yes-associated protein (YAP), a focal point of current biological research, is involved in regulating various life processes. In this report, live-cell fluorescence resonance energy transfer (FRET) imaging was employed to unravel the YAP complexes in MCF-7 cells. Fluorescence imaging of living cells co-expressing CFP (cyan fluorescent protein)-YAP and YFP (yellow fluorescent protein)-LATS1 (large tumor suppressor 1) plasmids revealed that YAP promoted LATS1 oligomerization around mitochondria.

View Article and Find Full Text PDF

Land plants alternate between asexual sporophytes and sexual gametophytes. Unlike seed plants, ferns develop free-living gametophytes. Gametophytes of the model fern Ceratopteris exhibit two sex types: hermaphrodites with pluripotent meristems and males lacking meristems.

View Article and Find Full Text PDF

One key determinant of HIV-1 latency reversal is the activation of the viral long terminal repeat (LTR) by cellular transcription factors such as NF-κB and AP-1. Interestingly, the activity of these two transcription factors can be modulated by glucocorticoid receptors (GRs). Furthermore, the HIV-1 genome contains multiple binding sites for GRs.

View Article and Find Full Text PDF

Unlabelled: Respiratory and encephalitic virus infections represent a significant risk to public health globally. Detailed investigations of immunological responses and disease outcomes during sequential virus infections are rare. Here, we define the impact of influenza virus infection on a subsequent virus encephalitis.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!