Paper Highlights

‘Yeast Mail’: A novel saccharomyces application (NSA) to encrypt messages

Helmut Rosemeyer, Achim Paululat, Jürgen J. Heinisch

Chem. Biodiversity 2014, DOI:10.1002/cbdv.201400160

The universal genetic code is used by all life forms to encode biological information. It can also be used to encrypt semantic messages and convey them within organisms without anyone but the sender and recipient knowing, i.e, as a means of steganography. Several theoretical, but comparatively few experimental, approaches have been dedicated to this subject, so far. Here, we describe an experimental system to stably integrate encrypted messages within the yeast genome using a polymerase chain reaction (PCR)-based, one-step homologous recombination system. Thus, DNA sequences encoding alphabetical and/or numerical information will be inherited by yeast propagation and can be sent in the form of dried yeast. Moreover, due to the availability of triple shuttle vectors, Saccharomyces cerevisiae can also be used as an intermediate construction device for transfer of information to either Drosophila or mammalian cells as steganographic containers. Besides its classical use in alcoholic fermentation and its modern use for heterologous gene expression, we here show that baker’s yeast can thus be employed in a novel Saccharomyces application (NSA) as a simple steganographic container to hide and convey messages.

 

RNA interference controlled by light of variable wavelength

Andreas Meyer, Andriy Mokhir

Angew. Chem. Int. Ed. 2014, DOI:10.1002/anie.201405885

Known “caged“ siRNAs are activated by UV light, which can be toxic to cells. An siRNAs that can be activated by red light under mild conditions is reported. The uncaging is mediated by 1O2 photo-generated by a photosensitizer, which is attached to the 3’-terminus of the lagging strand. The 5’-terminus of the guide strand is alkylated with a 9-anthracenyl residue.

 

Endless: A purine-binding RNA motif that can be expressed in cells

Christoph Kröner, Martin Thunemann, Sven Vollmer, Manuela Kinzer, Robert Feil, Clemens Richert

Angew. Chem. Int. Ed. 2014, DOI:10.1002/anie.201403579

A de novo designed RNA motif binds cGMP with low micromolar affinity and, when inducibly expressed in cells, acts as sink for this second messenger.

 

Influence of the absolute configuration of NPE-caged cytosine on DNA single base pair stability

H. S. Steinert, F. Schäfer, H. R. A. Jonker, A. Heckel, H. Schwalbe

Angew. Chem. Int. Ed. 2014, DOI:10.1002/anie.201307852

Photolabile protecting groups are a versatile tool to trigger reactions by light irradiation. In this study, we have investigated the influence of the absolute configuration of the 1-(2-nitrophenyl)ethyl (NPE) cage group on a 15-base-pair duplex DNA. Using UV melting, we determined the global stability of the unmodified and the selectively (S)- and (R)-NPE-modified DNA sequences, respectively. We observe a differently destabilizing effect for the two NPE stereoisomers on the global stability. Analysis of the temperature dependence of imino proton exchange rates measured by NMR spectroscopy reveals that this effect can be attributed to decreased base pair stabilities of the caged and the 3′-neighbouring base pair, respectively. Furthermore, our NMR based structural models of the modified duplexes provide a structural basis for the distinct effect of the (S)- and the (R)-NPE group.

 

Aptamer-guided caging for selective masking of protein domains

F. Rohrbach, F. Schäfer, M. A. H. Fichte, F. Pfeiffer, J. Müller, B. Pötzsch, A. Heckel, G. Mayer

Angew. Chem. Int. Ed. 2013, DOI:10.1002/anie.201306686

Photolabile protecting groups are a versatile tool to trigger reactions by light irradiation. In this study, we have investigated the influence of the absolute configuration of the 1-(2-nitrophenyl)ethyl (NPE) cage group on a 15-base-pair duplex DNA. Using UV melting, we determined the global stability of the unmodified and the selectively (S)- and (R)-NPE-modified DNA sequences, respectively. We observe a differently destabilizing effect for the two NPE stereoisomers on the global stability. Analysis of the temperature dependence of imino proton exchange rates measured by NMR spectroscopy reveals that this effect can be attributed to decreased base pair stabilities of the caged and the 3′-neighbouring base pair, respectively. Furthermore, our NMR based structural models of the modified duplexes provide a structural basis for the distinct effect of the (S)- and the (R)-NPE group.

 

A nucleobase analogue that pairs strongly with adenine

M. Minuth, C. Richert

Angew. Chem. Int. Ed. 2013, DOI:/10.1002/anie.201305555

Adenin war bisher schwer zu binden. Ein 6-Ethinyl-2-pyridon-C-Nucleosid paart mit hoher Affinität und Selektivität mit A in DNA- und RNA-Zielsträngen.