Comparing Agent-Based Delivery of DNA and PNA Forced Intercalation (FIT) Probes for Multicolor mRNA Imaging.
Jasmine ChamioloGe-Min FangFelix HövelmannDhana FriedrichAndrea KnollAlexander LöwerOliver SeitzPublished in: Chembiochem : a European journal of chemical biology (2018)
Fluorogenic oligonucleotide probes allow mRNA imaging in living cells. A key challenge is the cellular delivery of probes. Most delivery agents, such as cell-penetrating peptides (CPPs) and pore-forming proteins, require interactions with the membrane. Charges play an important role. To explore the influence of charge on fluorogenic properties and delivery efficiency, we compared peptide nucleic acid (PNA)- with DNA-based forced intercalation (FIT) probes. Perhaps counterintuitively, fluorescence signaling by charged DNA FIT probes proved tolerant to CPP conjugation, whereas CPP-FIT PNA conjugates were affected. Live-cell imaging was performed with a genetically engineered HEK293 cell line to allow the inducible expression of a specific mRNA target. Blob-like features and high background were recurring nuisances of the tested CPP and lipid conjugates. By contrast, delivery by streptolysin-O provided high enhancements of the fluorescence of the FIT probe upon target induction. Notably, DNA-based FIT probes were brighter and more responsive than PNA-based FIT probes. Optimized conditions enabled live-cell multicolor imaging of three different mRNA target sequences.
Keyphrases
- nucleic acid
- living cells
- single molecule
- high resolution
- fluorescent probe
- fluorescence imaging
- small molecule
- binding protein
- poor prognosis
- circulating tumor
- computed tomography
- magnetic resonance
- fatty acid
- stem cells
- photodynamic therapy
- mesenchymal stem cells
- cell therapy
- mass spectrometry
- energy transfer
- genetic diversity