Evidence map›Paper›PMID 31885202›Full record

ArticleMolecular systems biology2019

R2-P2 rapid-robotic phosphoproteomics enables multidimensional cell signaling studies.

Mario Leutert, Ricard A Rodríguez-Mias, Noelle K Fukuda, Judit Villén

Open access · goldAbstract read
In one paragraph

Article in Molecular systems biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 112 papers.

0numbers the graph read from it
0cells of the map it votes in
112citing papers in PubMed
9.0field-weighted citation impact, top 1% 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

112 citing papers in PubMed, 200 citations in OpenAlex.

  1. Article
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52 more citing papers are in PubMed but not listed here.

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

4 authors at 1 institution in 1 country.

Mario LeutertDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.ORCID 0000-0001-7921-4017
Ricard A Rodríguez-MiasDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.ORCID 0000-0001-7960-6387
Noelle K FukudaDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.ORCID 0000-0002-7609-0992
Judit VillénDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.ORCID 0000-0002-1005-1739
University of Washington · US

Funding

Emergent properties of signaling network degradation that mediate homeostatic failure during agingR01AG056359 · NIA · UNIVERSITY OF WASHINGTON · PI KAEBERLEIN, MATT, VILLEN, JUDIT · 2017 to 2021
$2.9M
Towards a comprehensive roadmap of cellular signaling.R35GM119536 · NIGMS · UNIVERSITY OF WASHINGTON · PI VILLEN, JUDIT · 2016 to 2020
$2.2M
NIA NIH HHS R01 AG056359NIGMS NIH HHS R35 GM119536
6 · The paper itself

Abstract

Recent developments in proteomics have enabled signaling studies where > 10,000 phosphosites can be routinely identified and quantified. Yet, current analyses are limited in throughput, reproducibility, and robustness, hampering experiments that involve multiple perturbations, such as those needed to map kinase-substrate relationships, capture pathway crosstalks, and network inference analysis. To address these challenges, we introduce rapid-robotic phosphoproteomics (R2-P2), an end-to-end automated method that uses magnetic particles to process protein extracts to deliver mass spectrometry-ready phosphopeptides. R2-P2 is rapid, robust, versatile, and high-throughput. To showcase the method, we applied it, in combination with data-independent acquisition mass spectrometry, to study signaling dynamics in the mitogen-activated protein kinase (MAPK) pathway in yeast. Our results reveal broad and specific signaling events along the mating, the high-osmolarity glycerol, and the invasive growth branches of the MAPK pathway, with robust phosphorylation of downstream regulatory proteins and transcription factors. Our method facilitates large-scale signaling studies involving hundreds of perturbations opening the door to systems-level studies aiming to capture signaling complexity.

Indexed as

Fungal ProteinsHigh-Throughput Screening AssaysMagnetic PhenomenaMAP Kinase Signaling SystemMass SpectrometryPhosphoproteinsProteomicsReproducibility of ResultsRoboticsYeastsFungal ProteinsPhosphoproteinsDIAMAPKmass spectrometryphosphoproteomicssignaling

Identifiers

PMID31885202
PMCPMC6920700
OpenAlexW2995512837

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.