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  High-resolution measurement of long-range distances in RNA: Pulse EPR spectroscopy with TEMPO-labeled nucleotides.

Halbmair, K., Seikowski, J., Tkach, I., Höbartner, C., Sezer, D., & Bennati, M. (2016). High-resolution measurement of long-range distances in RNA: Pulse EPR spectroscopy with TEMPO-labeled nucleotides. Chemical Science, 7(5), 3172-3180. doi:10.1039/C5SC04631A.

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Item Permalink: http://hdl.handle.net/11858/00-001M-0000-0029-CD82-B Version Permalink: http://hdl.handle.net/11858/00-001M-0000-002C-B28B-3
Genre: Journal Article

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Halbmair, K.1, Author              
Seikowski, J.2, Author              
Tkach, I.1, Author              
Höbartner, C.2, Author              
Sezer, D., Author
Bennati, M.1, Author              
Affiliations:
1Research Group of Electron Paramagnetic Resonance, MPI for biophysical chemistry, Max Planck Society, ou_578606              
2Research Group of Nucleic Acid Chemistry, MPI for Biophysical Chemistry, Max Planck Society, ou_578605              

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 Abstract: Structural information at atomic resolution of biomolecular assemblies, such as RNA and RNA protein complexes, is fundamental to comprehend biological function. Modern spectroscopic methods offer exceptional opportunities in this direction. Here we present the capability of pulse EPR to report high-resolution long-range distances in RNAs by means of a recently developed spin labeled nucleotide, which carries the TEMPO group directly attached to the nucleobase and preserves Watson–Crick base-pairing. In a representative RNA duplex with spin-label separations up to 28 base pairs (≈8 nm) we demonstrate that the label allows for a model-free conversion of inter-spin distances into base-pair separation (Δbp) if broad-band pulse excitation at Q band frequencies (34 GHz) is applied. The observed distance distribution increases from ±0.2 nm for Δbp = 10 to only ±0.5 nm for Δbp = 28, consistent with only small deviations from the “ideal” A-form RNA structure. Molecular dynamics (MD) simulations conducted at 20 °C show restricted conformational freedom of the label. MD-generated structural deviations from an “ideal” A-RNA geometry help disentangle the contributions of local flexibility of the label and its neighboring nucleobases and global deformations of the RNA double helix to the experimental distance distributions. The study demonstrates that our simple but strategic spin labeling procedure can access detailed structural information on RNAs at atomic resolution over distances that match the size of macromolecular RNA complexes.

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Language(s): eng - English
 Dates: 2016-02-03
 Publication Status: Published online
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 Rev. Method: Peer
 Identifiers: DOI: 10.1039/C5SC04631A
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Title: Chemical Science
Source Genre: Journal
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Pages: - Volume / Issue: 7 (5) Sequence Number: - Start / End Page: 3172 - 3180 Identifier: -