Synthesis of Selenium-modified RNA by engineered RNA Polymerases

• Antragsteller: Professor Dr. Andreas Marx
• Mitantragsteller: Professor Dr. Ronald Micura
• Fachliche Zuordnung: Biologische und Biomimetische Chemie
• Förderung: Förderung von 2009 bis 2015
• Projektkennung: Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 132770984

RNA is traditionally associated with the translational apparatus and is classified into three main categories that are mRNA, tRNA, and rRNA. However, in recent years, the important role of non-protein encoding RNAs (ncRNAs) has been recognized. The great number of ncRNAs and the growing interest into their functions are accompanied by the increasing demand for structural characterization. By far the most important method for nucleic acid structure determination is X-ray crystallography. Once crystals of a novel RNA have been grown and diffraction patterns recorded, phasing of the data can be a serious obstacle. To efficiently achieve this, modern techniques are available that require anomalous scattering centres within the respective RNA crystal. There are several options; one of them refers to Se-modified RNA whose chemical synthesis has been developed by one of us. However, preparation of Se-RNA by chemical solid-phase synthesis is highly time-consuming and the limitation with respect to the size of RNA represents another serious drawback at present. To overcome these hurdles we aim to develop an enzymatic synthesis strategy for Se-RNA using engineered RNA polymerases. By combining the strengths in organic chemistry, biotechnology and biochemistry of both groups in ribonucleotide synthesis and directed evolution of nucleic acid modifying enzymes, we will evolve new RNA polymerases that synthesize Se-modified RNA efficiently. Only in a collaboration of both groups the required broad methodologies and knowledge that are needed for the success of this project are available. While one group will put forward the chemical synthesis of 2’-methylseleno-modified triphosphates the other group will develop new means for the generation of RNA polymerase variants that accept the chemical modified nucleotides as substrate. The anticipated systems will provide large numbers of long RNAs that contain 2’-methylseleno-modified nucleotides for Xray analysis in an unprecedented short time span and thus spur progress along these lines.

• DFG-Verfahren: Sachbeihilfen
• Internationaler Bezug: Österreich