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Novel mass spectrometry methods for profiling modified RNA nucleotides in the nervous system

Award Information
Agency: Department of Health and Human Services
Branch: National Institutes of Health
Contract: 1R41DA038970-01
Agency Tracking Number: R41DA038970
Amount: $177,206.00
Phase: Phase I
Program: STTR
Solicitation Topic Code: NIDA
Solicitation Number: DA15-002
Timeline
Solicitation Year: 2014
Award Year: 2015
Award Start Date (Proposal Award Date): 2015-02-01
Award End Date (Contract End Date): 2016-01-31
Small Business Information
100 East Lancaster Avenue
Wynnewood, PA 19096-3450
United States
DUNS: 969728125
HUBZone Owned: No
Woman Owned: No
Socially and Economically Disadvantaged: No
Principal Investigator
 NIGEL WEBB
 (610) 801-2541
 nigel.webb@ribonova.com
Business Contact
 NIGEL WEBB
Phone: (610) 801-2541
Email: nigel.webb@ribonova.com
Research Institution
 UNIVERSITY OF CINCINNATI
 
2624 CLIFTON AVE
CINCINNATI, OH 45221-0001
United States

 Nonprofit College or University
Abstract

DESCRIPTION provided by applicant Pseudouridine is the most abundant post transcriptionally modified nucleoside found in ribonucleic acid RNA Pseudouridine is an enzymatically generated isomer of the canonical base uridine with additional hydrogen bonding capabilities and appears to lead to local structural and biochemical effects within RNAs Pseudouridine has been detected in several types of RNA including ribosomal RNA rRNA transfer RNA tRNA small nuclear RNA snRNA and may be present in messenger RNA mRNA The prevalence of pseudouridine appears to track its biological importance It has been implicated in a wide variety of cellular processes including gene expression gene regulation and steroid receptor signaling through pseudouridylation of the steroid receptor RNA activator SRA The role of pseudouridine in gene expression is mediated through the stabilization of codon anticodon interactions within the ribosome read through of stop codons through unusual base pairing attenuation of gene expression stress induced alternative splicing rRNA stability and ribosome assembly Recent results demonstrate that pseudouridine in mRNA can be translated by the ribosome The current interest in determining the medical significance of post transcriptionally modified nucleosides in RNA requires a new method that is capable of rapidly and conveniently identifying pseudouridine quantifying this modified nucleoside and determining its location within large RNA molecules This proposal seeks to conduct the necessary proof of concept experiments to develop a mass spectrometry MS based selected reaction monitoring SRM assay for pseudouridine that can be used to detect and localize this modified nucleoside within mammalian RNAs including RNAs from cells in the nervous system The proposed research plan addresses two aims Definition of technical specifications for the SRM assay including limits of detection and quantification dynamic range complexity of RNA sample and accuracy of pseudouridine detection quantification and sequence placement and Demonstration of the utility of this assay for monitoring this critical
modified nucleoside in human RNAs obtained from cell lines and tissue samples The research will also define the appropriate sample preparation steps required for turn key analysis of RNA by the MS based SRM assay Success in this project will support the development of a reagent kit for use by the scientific community to investigate the clinical significance of this most prevalent RNA modification The project will also examine the applicability of this assay to biopsy materials which could enable its use for research into a wide range of disorders of the nervous system

PUBLIC HEALTH RELEVANCE Pseudouridine is the most abundant post transcriptionally modified nucleoside found in ribonucleic acids This project will conduct the necessary proof of concept experiments to develop a mass spectrometry based assay for pseudouridine that can be used to detect quantify and locate this modified nucleoside in RNAs from a variety of mammalian cells Success in this project will enable the development of a reagent kit for use by the medical research community to investigate the clinical significance of this prevalent RNA modification in a wide range of disorders of the nervous system

* Information listed above is at the time of submission. *

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