Evidence map›Paper›PMID 31241912›Full record

ArticleAnalytical chemistry2019

Automated Nanoflow Two-Dimensional Reversed-Phase Liquid Chromatography System Enables In-Depth Proteome and Phosphoproteome Profiling of Nanoscale Samples.

Maowei Dou, Chia-Feng Tsai, Paul D Piehowski, Yang Wang, Thomas L Fillmore, Rui Zhao, Ronald J Moore, Pengfei Zhang, Wei-Jun Qian, Richard D Smith and 4 more

Open access · greenAbstract read
In one paragraph

Article in Analytical chemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

23 citing papers in PubMed, 47 citations in OpenAlex.

  1. Review
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  7. Single-nucleus proteomics identifies regulators of protein transport.bioRxiv : the preprint server for biology · 2024
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  12. Bottom-Up Proteomics: Advancements in Sample Preparation.International journal of molecular sciences · 2023
    Review
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  20. Single-cell Proteomics: Progress and Prospects.Molecular & cellular proteomics : MCP · 2020
    Review
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

14 authors at 2 institutions in 1 country.

Maowei DouEnvironmental Molecular Sciences Laboratory , Pacific Northwest National Laboratory , Richland , Washington 99354 , United States.
Chia-Feng TsaiBiological Sciences Division , Pacific Northwest National Laboratory , Richland , Washington 99354 , United States.ORCID 0000-0002-6514-6911
Paul D PiehowskiBiological Sciences Division , Pacific Northwest National Laboratory , Richland , Washington 99354 , United States.
Yang WangBiological Sciences Division , Pacific Northwest National Laboratory , Richland , Washington 99354 , United States.
Thomas L FillmoreEnvironmental Molecular Sciences Laboratory , Pacific Northwest National Laboratory , Richland , Washington 99354 , United States.
Rui ZhaoEnvironmental Molecular Sciences Laboratory , Pacific Northwest National Laboratory , Richland , Washington 99354 , United States.
Ronald J MooreBiological Sciences Division , Pacific Northwest National Laboratory , Richland , Washington 99354 , United States.ORCID 0000-0003-2806-2855
Pengfei ZhangBiological Sciences Division , Pacific Northwest National Laboratory , Richland , Washington 99354 , United States.
Wei-Jun QianBiological Sciences Division , Pacific Northwest National Laboratory , Richland , Washington 99354 , United States.ORCID 0000-0002-5393-2827
Richard D SmithBiological Sciences Division , Pacific Northwest National Laboratory , Richland , Washington 99354 , United States.
Tao LiuBiological Sciences Division , Pacific Northwest National Laboratory , Richland , Washington 99354 , United States.ORCID 0000-0001-9529-6550
Ryan T KellyEnvironmental Molecular Sciences Laboratory , Pacific Northwest National Laboratory , Richland , Washington 99354 , United States.ORCID 0000-0002-3339-4443
Tujin ShiBiological Sciences Division , Pacific Northwest National Laboratory , Richland , Washington 99354 , United States.ORCID 0000-0002-5592-3588
Ying ZhuEnvironmental Molecular Sciences Laboratory , Pacific Northwest National Laboratory , Richland , Washington 99354 , United States.ORCID 0000-0002-5416-0566
Pacific Northwest National Laboratory · USBrigham Young University · US

Funding

Equipment Supplement Request for a Research Resource for Ultra-sensitive High Throughput ProteomicsP41GM103493 · NIGMS · BATTELLE PACIFIC NORTHWEST LABORATORIES · PI SMITH, RICHARD D · 2012 to 2022
$22.6M
PNNL Proteome Characterization CenterU24CA210955 · NCI · BATTELLE PACIFIC NORTHWEST LABORATORIES · PI LIU, TAO, SMITH, RICHARD D · 2016 to 2020
$5.3M
Serum protein biomarkers for predicting type 1 diabetesDP3DK110844 · NIDDK · BATTELLE PACIFIC NORTHWEST LABORATORIES · PI QIAN, WEI-JUN · 2016 to 2016
$1.8M
Area A: In-Depth Proteome Mapping of the Tumor Microenvironment with Single-Cell ResolutionR33CA225248 · NCI · BRIGHAM YOUNG UNIVERSITY · PI KELLY, RYAN T · 2017 to 2017
$1.7M
An ultrasensitive targeted mass spectrometry system for proteomics analysis of single cellsR21CA223715 · NCI · BATTELLE PACIFIC NORTHWEST LABORATORIES · PI SHI, TUJIN · 2018 to 2020
$691k
NCI NIH HHS R21 CA223715NCI NIH HHS R33 CA225248NCI NIH HHS U24 CA210955NIDDK NIH HHS DP3 DK110844NIGMS NIH HHS P41 GM103493
6 · The paper itself

Abstract

Two-dimensional reversed-phase capillary liquid chromatography (2D RPLC) separations have enabled comprehensive proteome profiling of biological systems. However, milligram sample quantities of proteins are typically required due to significant losses during offline fractionation. Such a large sample requirement generally precludes the application samples in the nanogram to low-microgram range. To achieve in-depth proteomic analysis of such small-sized samples, we have developed the nanoFAC (nanoflow Fractionation and Automated Concatenation) 2D RPLC platform, in which the first dimension high-pH fractionation was performed on a 75-μm i.d. capillary column at a 300 nL/min flow rate with automated fraction concatenation, instead of on a typically used 2.1 mm column at a 200 μL/min flow rate with manual concatenation. Each fraction was then fully transferred to the second-dimension low-pH nanoLC separation using an autosampler equipped with a custom-machined syringe. We have found that using a polypropylene 96-well plate as collection device as well as the addition of

Indexed as

AutomationChromatography, Reverse-PhaseHeLa CellsHumansHydrogen-Ion ConcentrationMCF-7 CellsNanotechnologyPhosphoproteinsShewanellaPhosphoproteins

Identifiers

PMID31241912
PMCPMC6741344
OpenAlexW2955043776

What OpenQuestion holds

Textmetadata
LicenceTDM
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.