Evidence map›Paper›PMID 36732331›Full record

ArticleNature communications2023

Sample multiplexing-based targeted pathway proteomics with real-time analytics reveals the impact of genetic variation on protein expression.

Qing Yu, Xinyue Liu, Mark P Keller, Jose Navarrete-Perea, Tian Zhang, Sipei Fu, Laura P Vaites, Steven R Shuken, Ernst Schmid, Gregory R Keele and 9 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

24 citing papers in PubMed, 33 citations in OpenAlex.

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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

19 authors at 4 institutions in 1 country.

Qing YuDepartment of Cell Biology, Harvard Medical School, Boston, MA, 02115, USA.
Xinyue LiuDepartment of Cell Biology, Harvard Medical School, Boston, MA, 02115, USA.
Mark P KellerDepartment of Biochemistry, University of Wisconsin-Madison, Madison, WI, 53706, USA.ORCID 0000-0002-7405-5552
Jose Navarrete-PereaDepartment of Cell Biology, Harvard Medical School, Boston, MA, 02115, USA.
Tian ZhangDepartment of Cell Biology, Harvard Medical School, Boston, MA, 02115, USA.ORCID 0000-0001-9007-7965
Sipei FuDepartment of Cell Biology, Harvard Medical School, Boston, MA, 02115, USA.
Laura P VaitesDepartment of Cell Biology, Harvard Medical School, Boston, MA, 02115, USA.
Steven R ShukenDepartment of Cell Biology, Harvard Medical School, Boston, MA, 02115, USA.
Ernst SchmidDepartment of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA, 02115, USA.
Gregory R KeeleThe Jackson Laboratory, Bar Harbor, Maine, 04609, USA.ORCID 0000-0002-1843-7900
Jiaming LiDepartment of Cell Biology, Harvard Medical School, Boston, MA, 02115, USA.
Edward L HuttlinDepartment of Cell Biology, Harvard Medical School, Boston, MA, 02115, USA.ORCID 0000-0002-1822-1173
Edrees H RashanDepartment of Biochemistry, University of Wisconsin-Madison, Madison, WI, 53706, USA.
Judith SimcoxDepartment of Biochemistry, University of Wisconsin-Madison, Madison, WI, 53706, USA.ORCID 0000-0001-7350-6342
Gary A ChurchillThe Jackson Laboratory, Bar Harbor, Maine, 04609, USA.ORCID 0000-0001-9190-9284
Devin K SchweppeDepartment of Genome Sciences, University of Washington, Seattle, WA, 98105, USA.ORCID 0000-0002-3241-6276
Alan D AttieDepartment of Biochemistry, University of Wisconsin-Madison, Madison, WI, 53706, USA.ORCID 0000-0002-0568-2261
Joao A PauloDepartment of Cell Biology, Harvard Medical School, Boston, MA, 02115, USA.ORCID 0000-0002-4291-413X
Steven P GygiDepartment of Cell Biology, Harvard Medical School, Boston, MA, 02115, USA. Steven_Gygi@hms.harvard.edu.ORCID 0000-0001-7626-0034
Harvard University · USUniversity of Wisconsin–Madison · USJackson Laboratory · USUniversity of Washington · US

Funding

New Sample Multiplexing Technologies to Identify Chemical Probes and Illuminate Ubiquitin BiologyR01GM067945 · NIGMS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI GYGI, STEVEN P · 2003 to 2024
$10.5M
Genetic Control of Metabolic Flux in Response to DietRC2DK125961 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI ATTIE, ALAN D · 2020 to 2024
$8.1M
The Diversity Outbred Diabetes ProjectR01DK101573 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI Alan D Attie · 2014 to 2026
$5.3M
Advancing Multiplexed Isobaric Tag-based Strategies for Proteome ProfilingR01GM132129 · NIGMS · HARVARD MEDICAL SCHOOL · PI PAULO, JOAO A · 2019 to 2023
$1.7M
A new multi-pathway kinase activity assay applied to compound library screening in cancer biologyK99CA273170 · NCI · HARVARD MEDICAL SCHOOL · PI ZHANG, TIAN · 2022 to 2022
$117k
NCI NIH HHS K99 CA273170NIDDK NIH HHS R01 DK101573NIDDK NIH HHS RC2 DK125961NIGMS NIH HHS R01 GM067945NIGMS NIH HHS R01 GM132129
6 · The paper itself

Abstract

Targeted proteomics enables hypothesis-driven research by measuring the cellular expression of protein cohorts related by function, disease, or class after perturbation. Here, we present a pathway-centric approach and an assay builder resource for targeting entire pathways of up to 200 proteins selected from >10,000 expressed proteins to directly measure their abundances, exploiting sample multiplexing to increase throughput by 16-fold. The strategy, termed GoDig, requires only a single-shot LC-MS analysis, ~1 µg combined peptide material, a list of up to 200 proteins, and real-time analytics to trigger simultaneous quantification of up to 16 samples for hundreds of analytes. We apply GoDig to quantify the impact of genetic variation on protein expression in mice fed a high-fat diet. We create several GoDig assays to quantify the expression of multiple protein families (kinases, lipid metabolism- and lipid droplet-associated proteins) across 480 fully-genotyped Diversity Outbred mice, revealing protein quantitative trait loci and establishing potential linkages between specific proteins and lipid homeostasis.

Indexed as

ProteinsProteomicsAnimalsGenetic VariationMass SpectrometryMicePeptidesPeptidesProteins

Identifiers

PMID36732331
PMCPMC9894840
OpenAlexW4319032825

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.