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An analytical platform for mass spectrometry-based identification and chemical analysis of RNA in ribonucleoprotein complexes

We describe here a mass spectrometry (MS)-based analytical platform of RNA, which combines direct nano-flow reversed-phase liquid chromatography (RPLC) on a spray tip column and a high-resolution LTQ-Orbitrap mass spectrometer. Operating RPLC under a very low flow rate with volatile solvents and MS...

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Detalles Bibliográficos
Autores principales: Taoka, Masato, Yamauchi, Yoshio, Nobe, Yuko, Masaki, Shunpei, Nakayama, Hiroshi, Ishikawa, Hideaki, Takahashi, Nobuhiro, Isobe, Toshiaki
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2790879/
https://www.ncbi.nlm.nih.gov/pubmed/19740761
http://dx.doi.org/10.1093/nar/gkp732
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author Taoka, Masato
Yamauchi, Yoshio
Nobe, Yuko
Masaki, Shunpei
Nakayama, Hiroshi
Ishikawa, Hideaki
Takahashi, Nobuhiro
Isobe, Toshiaki
author_facet Taoka, Masato
Yamauchi, Yoshio
Nobe, Yuko
Masaki, Shunpei
Nakayama, Hiroshi
Ishikawa, Hideaki
Takahashi, Nobuhiro
Isobe, Toshiaki
author_sort Taoka, Masato
collection PubMed
description We describe here a mass spectrometry (MS)-based analytical platform of RNA, which combines direct nano-flow reversed-phase liquid chromatography (RPLC) on a spray tip column and a high-resolution LTQ-Orbitrap mass spectrometer. Operating RPLC under a very low flow rate with volatile solvents and MS in the negative mode, we could estimate highly accurate mass values sufficient to predict the nucleotide composition of a ∼21-nucleotide small interfering RNA, detect post-transcriptional modifications in yeast tRNA, and perform collision-induced dissociation/tandem MS-based structural analysis of nucleolytic fragments of RNA at a sub-femtomole level. Importantly, the method allowed the identification and chemical analysis of small RNAs in ribonucleoprotein (RNP) complex, such as the pre-spliceosomal RNP complex, which was pulled down from cultured cells with a tagged protein cofactor as bait. We have recently developed a unique genome-oriented database search engine, Ariadne, which allows tandem MS-based identification of RNAs in biological samples. Thus, the method presented here has broad potential for automated analysis of RNA; it complements conventional molecular biology-based techniques and is particularly suited for simultaneous analysis of the composition, structure, interaction, and dynamics of RNA and protein components in various cellular RNP complexes.
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spelling pubmed-27908792009-12-09 An analytical platform for mass spectrometry-based identification and chemical analysis of RNA in ribonucleoprotein complexes Taoka, Masato Yamauchi, Yoshio Nobe, Yuko Masaki, Shunpei Nakayama, Hiroshi Ishikawa, Hideaki Takahashi, Nobuhiro Isobe, Toshiaki Nucleic Acids Res Methods Online We describe here a mass spectrometry (MS)-based analytical platform of RNA, which combines direct nano-flow reversed-phase liquid chromatography (RPLC) on a spray tip column and a high-resolution LTQ-Orbitrap mass spectrometer. Operating RPLC under a very low flow rate with volatile solvents and MS in the negative mode, we could estimate highly accurate mass values sufficient to predict the nucleotide composition of a ∼21-nucleotide small interfering RNA, detect post-transcriptional modifications in yeast tRNA, and perform collision-induced dissociation/tandem MS-based structural analysis of nucleolytic fragments of RNA at a sub-femtomole level. Importantly, the method allowed the identification and chemical analysis of small RNAs in ribonucleoprotein (RNP) complex, such as the pre-spliceosomal RNP complex, which was pulled down from cultured cells with a tagged protein cofactor as bait. We have recently developed a unique genome-oriented database search engine, Ariadne, which allows tandem MS-based identification of RNAs in biological samples. Thus, the method presented here has broad potential for automated analysis of RNA; it complements conventional molecular biology-based techniques and is particularly suited for simultaneous analysis of the composition, structure, interaction, and dynamics of RNA and protein components in various cellular RNP complexes. Oxford University Press 2009-11 2009-09-09 /pmc/articles/PMC2790879/ /pubmed/19740761 http://dx.doi.org/10.1093/nar/gkp732 Text en © The Author(s) 2009. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.5/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methods Online
Taoka, Masato
Yamauchi, Yoshio
Nobe, Yuko
Masaki, Shunpei
Nakayama, Hiroshi
Ishikawa, Hideaki
Takahashi, Nobuhiro
Isobe, Toshiaki
An analytical platform for mass spectrometry-based identification and chemical analysis of RNA in ribonucleoprotein complexes
title An analytical platform for mass spectrometry-based identification and chemical analysis of RNA in ribonucleoprotein complexes
title_full An analytical platform for mass spectrometry-based identification and chemical analysis of RNA in ribonucleoprotein complexes
title_fullStr An analytical platform for mass spectrometry-based identification and chemical analysis of RNA in ribonucleoprotein complexes
title_full_unstemmed An analytical platform for mass spectrometry-based identification and chemical analysis of RNA in ribonucleoprotein complexes
title_short An analytical platform for mass spectrometry-based identification and chemical analysis of RNA in ribonucleoprotein complexes
title_sort analytical platform for mass spectrometry-based identification and chemical analysis of rna in ribonucleoprotein complexes
topic Methods Online
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2790879/
https://www.ncbi.nlm.nih.gov/pubmed/19740761
http://dx.doi.org/10.1093/nar/gkp732
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