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• W2156349934 abstract "We used a high flux synchrotron X-ray beam to map the structure of 16S rRNA and RNase P in viable bacteria in situ. A 300 ms exposure to the X-ray beam was sufficient for optimal cleavage of the phosphodiester backbone. The in vivo footprints of the 16S rRNA in frozen cells were similar to those obtained in vitro and were consistent with the predicted accessibility of the RNA backbone to hydroxyl radical. Protection or enhanced cleavage of certain nucleotides in vivo can be explained by interactions with tRNA and perturbation of the subunit interface. Thus, short exposures to a synchrotron X-ray beam can footprint the tertiary structure and protein contacts of RNA–protein complexes with nucleotide resolution in living cells." @default.
• W2156349934 created "2016-06-24" @default.
• W2156349934 creator A5004503902 @default.
• W2156349934 date "2006-04-28" @default.
• W2156349934 modified "2023-09-29" @default.
• W2156349934 title "Hydroxyl radical footprinting in vivo: mapping macromolecular structures with synchrotron radiation" @default.
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• W2156349934 doi "https://doi.org/10.1093/nar/gkl291" @default.
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