The method is based on a new molecular marker called the rhodamine-binding aptamer for methods
RhoBAST is developed by researchers from the InstitutePharmacy and Molecular Biotechnology (IPMB) of the University of Heidelberg and the Institute for Applied Physics (APH) at KIT. The marker they created is genetically encoded, which means that it can be fused with the gene of any RNA produced by the cell. RhoBAST itself is not fluorescent, but illuminates the cell-permeable rhodamine dye by binding to it in a very specific manner.
“This leads to a dramatic increase in fluorescence,achievable with the RhoBAST complex, which is a key requirement for superior fluorescence imaging. However, to visualize ultra-high resolution RNA, the marker needs additional properties. "
Murat Zünbühl from IPMB
The researchers found that each moleculethe rhodamine dye remains bound to RhoBAST for only about one second before detaching again. After a few seconds, this procedure is repeated with a new dye molecule. It is quite rare to find strong interactions, for example, between RhoBAST and rhodamine, combined with extremely fast metabolic kinetics. Since rhodamine only lights up after binding to RhoBAST, the constant sequence of re-emerging interactions between the marker and the dye leads to continuous “blinking”. This on-off is exactly what you need for rendering.
At the same time, the RhoBAST system solves anotheran important problem. Fluorescent images are collected by exposure to laser light, which over time breaks down the dye molecules. Rapid dye change ensures that photobleached dyes are replaced with fresh ones. This means that individual RNA molecules can be observed for longer periods of time, which can significantly improve image resolution.
Researchers from Heidelberg and Karlsruhe were able todemonstrate the superior properties of RhoBAST by visualizing RNA structures within intestinal bacteria (Escherichia coli) and cultured human cells with superior localization accuracy. Scientists were able to uncover details of previously invisible subcellular structures and molecular interactions involving RNA using ultra-high-resolution fluorescence microscopy. This will provide a fundamentally new understanding of biological processes.
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