Posttranscriptional modifications in ribosomal ribonucleic acids (rRNAs) are difficult to identify and their function is unknown. Our knowledge of the functional role of these posttranscriptional modifications is limited largely by the lack of methods for their routine identification. The long-term goal of our research has been and continues to be to develop appropriate mass spectrometric approaches to characterize the structure of the ribosome in terms of RNA. The goal of this funding period will be to extend our previous improvements in mass spectrometric methods for identifying posttranscriptional modifications in rRNA in order to permit the structural interactions between (modified) nucleosides in rRNA and ribosomal proteins to be characterized. We will develop new, improved mass spectrometry (MS) methods to characterize ribonucleoprotein (RNP) interactions within the ribosome. We will use matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) to identify cross-links between RNA and ribosomal proteins. We will extend our current developments using RNase H to digest rRNAs to focus on particular regions of the ribosome as a means of simplifying the determination of protein:nucleic acid cross-links. In particular, we will use this new approach to focus on areas of rRNA known to contain posttranscriptionally modified nucleosides to ascertain the structural significance of such modifications. We will use limited proteolysis with MALDI-MS to characterize ribosome organization, topology and proteins suspected of directly interacting with rRNA. Limited proteolysis, cross-linking and analysis by MALDI-MS and liquid chromatography mass spectrometry will be used to identify sites of interaction between ribosomal proteins and rRNAs suspected of being important in ribosome assembly. As pseudouridine is the most common posttranscriptionally modified nucleoside, we propose to develop an improved method for identifying this modification and analyzing its role in rRNA:rRNA and rRNA:protein interactions. Furthermore, we will apply advances in method developments in proteomics to initiate studies aimed at characterizing the structural interactions of bacterial ribosomes as a function of cell growth conditions. These latter studies will open up new avenues of research in characterizing the dynamic nature of the ribosome. In addition, this research will facilitate future studies that will help determine how ribosomes can carry.out the task of translation with amazing speed and accuracy. ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM058843-07
Application #
7151226
Study Section
Special Emphasis Panel (ZRG1-BECM (01))
Program Officer
Edmonds, Charles G
Project Start
1999-02-01
Project End
2008-11-30
Budget Start
2006-12-01
Budget End
2007-11-30
Support Year
7
Fiscal Year
2007
Total Cost
$245,868
Indirect Cost
Name
University of Cincinnati
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
041064767
City
Cincinnati
State
OH
Country
United States
Zip Code
45221
Ross, Robert L; Cao, Xiaoyu; Limbach, Patrick A (2017) Mapping Post-Transcriptional Modifications onto  Transfer Ribonucleic Acid Sequences by Liquid  Chromatography Tandem Mass Spectrometry. Biomolecules 7:
Rubio, Mary Anne T; Gaston, Kirk W; McKenney, Katherine M et al. (2017) Editing and methylation at a single site by functionally interdependent activities. Nature 542:494-497
Limbach, Patrick A; Paulines, Mellie June (2017) Going global: the new era of mapping modifications in RNA. Wiley Interdiscip Rev RNA 8:
Addepalli, Balasubrahmanyam; Venus, Sarah; Thakur, Priti et al. (2017) Novel ribonuclease activity of cusativin from Cucumis sativus for mapping nucleoside modifications in RNA. Anal Bioanal Chem 409:5645-5654
Wetzel, Collin; Limbach, Patrick A (2016) Mass spectrometry of modified RNAs: recent developments. Analyst 141:16-23
Addepalli, Balasubrahmanyam; Limbach, Patrick A (2016) Pseudouridine in the Anticodon of Escherichia coli tRNATyr(Q?A) Is Catalyzed by the Dual Specificity Enzyme RluF. J Biol Chem 291:22327-22337
Ross, Robert; Cao, Xiaoyu; Yu, Ningxi et al. (2016) Sequence mapping of transfer RNA chemical modifications by liquid chromatography tandem mass spectrometry. Methods 107:73-8
Addepalli, Balasubrahmanym; Lesner, Nicholas P; Limbach, Patrick A (2015) Detection of RNA nucleoside modifications with the uridine-specific ribonuclease MC1 from Momordica charantia. RNA 21:1746-56
Cao, Xiaoyu; Limbach, Patrick A (2015) Enhanced detection of post-transcriptional modifications using a mass-exclusion list strategy for RNA modification mapping by LC-MS/MS. Anal Chem 87:8433-40
Sample, Paul J; Gaston, Kirk W; Alfonzo, Juan D et al. (2015) RoboOligo: software for mass spectrometry data to support manual and de novo sequencing of post-transcriptionally modified ribonucleic acids. Nucleic Acids Res 43:e64

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