Evidence map›Paper›PMID 29055021›Full record

ArticleMolecular & cellular proteomics : MCP2017

MEERCAT: Multiplexed Efficient Cell Free Expression of Recombinant QconCATs For Large Scale Absolute Proteome Quantification.

Nobuaki Takemori, Ayako Takemori, Yuki Tanaka, Yaeta Endo, Jane L Hurst, Guadalupe Gómez-Baena, Victoria M Harman, Robert J Beynon

Open access · hybridAbstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.7field-weighted citation impact, top 30% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 30 citations in OpenAlex.

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  13. Proteomic/transcriptomic analysis of erythropoiesis.Current opinion in hematology · 2021
    Review
  14. Review
  15. Development of a cell-free protein synthesis system for practical use.Proceedings of the Japan Academy. Series B, Physical and biological sciences · 2021
    Article
  16. Social status and ejaculate composition in the house mouse.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2020
    Article
  17. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 2 countries.

Nobuaki TakemoriFrom the ‡Proteo-Science Center, Ehime University, Ehime, 791-0295, Japan; r.beynon@liverpool.ac.uk takemori@m.ehime-u.ac.jp.
Ayako TakemoriFrom the ‡Proteo-Science Center, Ehime University, Ehime, 791-0295, Japan.
Yuki Tanaka§Advanced Research Support Center, Ehime University, Ehime, 791-0295, Japan.
Yaeta EndoFrom the ‡Proteo-Science Center, Ehime University, Ehime, 791-0295, Japan.
Jane L Hurst**Mammalian Behaviour and Evolution Group, Institute of Integrative Biology, University of Liverpool, Leahurst Campus, Neston CH64 7TE.
Guadalupe Gómez-Baena‖Centre for Proteome Research, Institute of Integrative Biology, University of Liverpool, Liverpool, L69 7ZB, UK.
Victoria M Harman‖Centre for Proteome Research, Institute of Integrative Biology, University of Liverpool, Liverpool, L69 7ZB, UK.
Robert J Beynon‖Centre for Proteome Research, Institute of Integrative Biology, University of Liverpool, Liverpool, L69 7ZB, UK; r.beynon@liverpool.ac.uk takemori@m.ehime-u.ac.jp.
Ehime University · JPUniversity of Liverpool · GB

Funding

Medical Research Council MR/M009114/1
6 · The paper itself

Abstract

A major challenge in proteomics is the absolute accurate quantification of large numbers of proteins. QconCATs, artificial proteins that are concatenations of multiple standard peptides, are well established as an efficient means to generate standards for proteome quantification. Previously, QconCATs have been expressed in bacteria, but we now describe QconCAT expression in a robust, cell-free system. The new expression approach rescues QconCATs that previously were unable to be expressed in bacteria and can reduce the incidence of proteolytic damage to QconCATs. Moreover, it is possible to cosynthesize QconCATs in a highly-multiplexed translation reaction, coexpressing tens or hundreds of QconCATs simultaneously. By obviating bacterial culture and through the gain of high level multiplexing, it is now possible to generate tens of thousands of standard peptides in a matter of weeks, rendering absolute quantification of a complex proteome highly achievable in a reproducible, broadly deployable system.

Indexed as

Base SequenceCell-Free SystemGene LibraryHumansIsotope LabelingPeptidesProteomeProteomicsTandem Mass SpectrometryPeptidesProteome

Identifiers

PMID29055021
PMCPMC5724179
OpenAlexW2765342059

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.