Proteomics

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Differential stoichiometry among core ribosomal proteins


ABSTRACT: Understanding the regulation and structure of ribosomes is essential to understanding protein synthesis and its dysregulation in disease. While ribosomes are believed to have a fixed stoichiometry among their core ribosomal proteins (RPs), some experiments suggest a more variable composition. Testing such variability requires direct and precise quantification of RPs. We used mass-spectrometry to directly quantify RPs across monosomes and polysomes of mouse embryonic stem cells (ESC) and budding yeast. Our data show that the stoichiometry among core RPs in wild-type yeast cells and ESC depends both on the growth conditions and on the number of ribosomes bound per mRNA. Furthermore, we find that the fitness of cells with a deleted RP-gene is inversely proportional to the enrichment of the corresponding RP in polysomes. Together, our findings support the existence of ribosomes with distinct protein composition and physiological function.

INSTRUMENT(S): LTQ Orbitrap Elite

ORGANISM(S): Saccharomycetales (ncbitaxon:4892) Mus Musculus (ncbitaxon:10090)

SUBMITTER: Nikolai Slavov 

PROVIDER: MSV000079280 | MassIVE | Fri Aug 28 12:21:00 BST 2015

SECONDARY ACCESSION(S): PXD002816

REPOSITORIES: MassIVE

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Differential Stoichiometry among Core Ribosomal Proteins.

Slavov Nikolai N   Semrau Stefan S   Airoldi Edoardo E   Budnik Bogdan B   van Oudenaarden Alexander A  

Cell reports 20151022 5


Understanding the regulation and structure of ribosomes is essential to understanding protein synthesis and its dysregulation in disease. While ribosomes are believed to have a fixed stoichiometry among their core ribosomal proteins (RPs), some experiments suggest a more variable composition. Testing such variability requires direct and precise quantification of RPs. We used mass spectrometry to directly quantify RPs across monosomes and polysomes of mouse embryonic stem cells (ESC) and budding  ...[more]

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