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ARiBo pull-down for riboproteomic studies based on label-free quantitative mass spectrometry
As part of their normal life cycle, most RNA molecules associate with several proteins that direct their fate and regulate their function. Here, we describe a novel method for identifying proteins that associate with a target RNA. The procedure is based on the ARiBo method for affinity purification...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5066628/ https://www.ncbi.nlm.nih.gov/pubmed/27659051 http://dx.doi.org/10.1261/rna.057513.116 |
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author | Di Tomasso, Geneviève Miller Jenkins, Lisa M. Legault, Pascale |
author_facet | Di Tomasso, Geneviève Miller Jenkins, Lisa M. Legault, Pascale |
author_sort | Di Tomasso, Geneviève |
collection | PubMed |
description | As part of their normal life cycle, most RNA molecules associate with several proteins that direct their fate and regulate their function. Here, we describe a novel method for identifying proteins that associate with a target RNA. The procedure is based on the ARiBo method for affinity purification of RNA, which was originally developed to quickly purify RNA with high yields and purity under native conditions. The ARiBo method was further optimized using in vitro transcribed RNA to capture RNA-associating proteins from cellular extracts with high yields and low background protein contamination. For these RNA pull-downs, stem–loops present in the immature forms of let-7 miRNAs (miRNA stem–loops) were used as the target RNAs. Label-free quantitative mass spectrometry analysis allowed for the reliable identification of proteins that are specific to the stem–loops present in the immature forms of two miRNAs, let-7a-1 and let-7g. Several proteins known to bind immature forms of these let-7 miRNAs were identified, but with an improved coverage compared to previous studies. In addition, several novel proteins were identified that better define the protein interactome of the let-7 miRNA stem–loops and further link let-7 biogenesis to important biological processes such as development and tumorigenesis. Thus, combining the ARiBo pull-down method with label-free quantitative mass spectrometry provides an effective proteomic approach for identification of proteins that associate with a target RNA. |
format | Online Article Text |
id | pubmed-5066628 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-50666282016-11-01 ARiBo pull-down for riboproteomic studies based on label-free quantitative mass spectrometry Di Tomasso, Geneviève Miller Jenkins, Lisa M. Legault, Pascale RNA Method As part of their normal life cycle, most RNA molecules associate with several proteins that direct their fate and regulate their function. Here, we describe a novel method for identifying proteins that associate with a target RNA. The procedure is based on the ARiBo method for affinity purification of RNA, which was originally developed to quickly purify RNA with high yields and purity under native conditions. The ARiBo method was further optimized using in vitro transcribed RNA to capture RNA-associating proteins from cellular extracts with high yields and low background protein contamination. For these RNA pull-downs, stem–loops present in the immature forms of let-7 miRNAs (miRNA stem–loops) were used as the target RNAs. Label-free quantitative mass spectrometry analysis allowed for the reliable identification of proteins that are specific to the stem–loops present in the immature forms of two miRNAs, let-7a-1 and let-7g. Several proteins known to bind immature forms of these let-7 miRNAs were identified, but with an improved coverage compared to previous studies. In addition, several novel proteins were identified that better define the protein interactome of the let-7 miRNA stem–loops and further link let-7 biogenesis to important biological processes such as development and tumorigenesis. Thus, combining the ARiBo pull-down method with label-free quantitative mass spectrometry provides an effective proteomic approach for identification of proteins that associate with a target RNA. Cold Spring Harbor Laboratory Press 2016-11 /pmc/articles/PMC5066628/ /pubmed/27659051 http://dx.doi.org/10.1261/rna.057513.116 Text en © 2016 Di Tomasso et al.; Published by Cold Spring Harbor Laboratory Press for the RNA Society http://creativecommons.org/licenses/by-nc/4.0/ This article, published in RNA, is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Method Di Tomasso, Geneviève Miller Jenkins, Lisa M. Legault, Pascale ARiBo pull-down for riboproteomic studies based on label-free quantitative mass spectrometry |
title | ARiBo pull-down for riboproteomic studies based on label-free quantitative mass spectrometry |
title_full | ARiBo pull-down for riboproteomic studies based on label-free quantitative mass spectrometry |
title_fullStr | ARiBo pull-down for riboproteomic studies based on label-free quantitative mass spectrometry |
title_full_unstemmed | ARiBo pull-down for riboproteomic studies based on label-free quantitative mass spectrometry |
title_short | ARiBo pull-down for riboproteomic studies based on label-free quantitative mass spectrometry |
title_sort | aribo pull-down for riboproteomic studies based on label-free quantitative mass spectrometry |
topic | Method |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5066628/ https://www.ncbi.nlm.nih.gov/pubmed/27659051 http://dx.doi.org/10.1261/rna.057513.116 |
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