Dataset Information

Novel proteomic approach (PUNCH-P) reveals cell cycle-specific fluctuations in mRNA translation

ABSTRACT: Monitoring protein synthesis is essential to our understanding of gene expression regulation, as protein abundance is thought to be predominantly controlled at the level of translation. Mass-spectrometric and RNA sequencing methods have been recently developed for investigating mRNA translation at a global level, but these still involve technical limitations and are not widely applicable. In this study, we describe a novel system-wide proteomic approach for direct monitoring of translation, termed puromycin-associated nascent chain proteomics (PUNCH-P), which is based on incorporation of biotinylated puromycin into newly synthesized proteins under cell-free conditions followed by streptavidin affinity purification and liquid chromatography-tandem mass spectrometry analysis. Using PUNCH-P, we measured cell cycle-specific fluctuations in synthesis for >5000 proteins in mammalian cells, identified proteins not previously implicated in cell cycle processes, and generated the first translational profile of a whole mouse brain. This simple and economical technique is broadly applicable to any cell type and tissue, enabling the identification and quantification of rapid proteome responses under various biological conditions.

INSTRUMENT(S): Q Exactive

ORGANISM(S): Homo Sapiens (human)

TISSUE(S): Epithelial Cell, Hela Cell

DISEASE(S): Cervix Carcinoma

SUBMITTER: Tamar Geiger

LAB HEAD: Tamar Geiger

PROVIDER: PXD012727 | Pride | 2019-02-18

REPOSITORIES: Pride

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			Action	DRS
	20130613_TG_SA_COLLAB_Ranen_Em1.raw	Raw
	20130613_TG_SA_COLLAB_Ranen_Em2.raw	Raw
	20130613_TG_SA_COLLAB_Ranen_Em3.raw	Raw
	20130613_TG_SA_COLLAB_Ranen_ctr1.raw	Raw
	20130613_TG_SA_COLLAB_Ranen_ctr2.raw	Raw

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Novel proteomic approach (PUNCH-P) reveals cell cycle-specific fluctuations in mRNA translation.

Aviner Ranen R Geiger Tamar T Elroy-Stein Orna O

Genes & development 20130809 16

Monitoring protein synthesis is essential to our understanding of gene expression regulation, as protein abundance is thought to be predominantly controlled at the level of translation. Mass-spectrometric and RNA sequencing methods have been recently developed for investigating mRNA translation at a global level, but these still involve technical limitations and are not widely applicable. In this study, we describe a novel system-wide proteomic approach for direct monitoring of translation, term ...[more]

PMID: 23934657

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