Evidence map›Paper›PMID 23763644›Full record

ArticleJournal of proteome research2013

Targeted quantification of low ng/mL level proteins in human serum without immunoaffinity depletion.

Tujin Shi, Xuefei Sun, Yuqian Gao, Thomas L Fillmore, Athena A Schepmoes, Rui Zhao, Jintang He, Ronald J Moore, Jacob Kagan, Karin D Rodland and 6 more

Abstract read
In one paragraph

Article in Journal of proteome research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
–field-weighted citation impact
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

35 citing papers in PubMed.

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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

16 authors.

Tujin ShiBiological Sciences Division, Pacific Northwest National Laboratory, Richland, Washington, USA.
Xuefei Sun
Yuqian Gao
Thomas L Fillmore
Athena A Schepmoes
Rui Zhao
Jintang He
Ronald J Moore
Jacob Kagan
Karin D Rodland
Tao Liu
Alvin Y Liu
Richard D Smith
Keqi Tang
David G Camp
Wei-Jun Qian

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 Clinical Proteome Characterization CenterU24CA160019 · NCI · BATTELLE PACIFIC NORTHWEST LABORATORIES · PI RODLAND, KARIN D, SMITH, RICHARD D · 2011 to 2016
$15.7M
The Early Detection Research Network: Biomarker Developmental LaboratoriesU01CA111244 · NCI · UNIVERSITY OF WASHINGTON · PI LIU, ALVIN Y · 2004 to 2015
$4.1M
A Universal Multiplex Assay System for High-Throughput Clinical ApplicationsDP2OD006668 · OD · BATTELLE PACIFIC NORTHWEST LABORATORIES · PI QIAN, WEI-JUN · 2009 to 2009
$2.1M
Validation and Advanced Development of Emerging TechnologiesR33CA155252 · NCI · BATTELLE PACIFIC NORTHWEST LABORATORIES · PI TANG, KEQI · 2011 to 2013
$1.3M
NCI NIH HHS R33 CA155252NCI NIH HHS R33CA155252NCI NIH HHS U01 CA111244NCI NIH HHS U01CA111244NCI NIH HHS U24 CA160019NCI NIH HHS U24CA160019NCI NIH HHS Y01CN05013-29NIGMS NIH HHS P41 GM103493NIGMS NIH HHS P41GM103493NIH HHS DP2 OD006668NIH HHS DP2OD006668
6 · The paper itself

Abstract

We recently reported an antibody-free targeted protein quantification strategy, termed high-pressure, high-resolution separations with intelligent selection and multiplexing (PRISM), for achieving significantly enhanced sensitivity using selected reaction monitoring (SRM) mass spectrometry. Integrating PRISM with front-end IgY14 immunoaffinity depletion, sensitive detection of targeted proteins at 50-100 pg/mL levels in human blood plasma/serum was demonstrated. However, immunoaffinity depletion is often associated with undesired losses of target proteins of interest. Herein we report further evaluation of PRISM-SRM quantification of low-abundance serum proteins without immunoaffinity depletion. Limits of quantification (LOQ) at low ng/mL levels with a median coefficient of variation (CV) of ∼12% were achieved for proteins spiked into human female serum. PRISM-SRM provided >100-fold improvement in the LOQ when compared to conventional LC-SRM measurements. PRISM-SRM was then applied to measure several low-abundance endogenous serum proteins, including prostate-specific antigen (PSA), in clinical prostate cancer patient sera. PRISM-SRM enabled confident detection of all target endogenous serum proteins except the low pg/mL-level cardiac troponin T. A correlation coefficient >0.99 was observed for PSA between the results from PRISM-SRM and immunoassays. Our results demonstrate that PRISM-SRM can successfully quantify low ng/mL proteins in human plasma or serum without depletion. We anticipate broad applications for PRISM-SRM quantification of low-abundance proteins in candidate biomarker verification and systems biology studies.

Indexed as

BiomarkersBlood ProteinsChromatography, LiquidFemaleHumansLimit of DetectionMaleMass SpectrometryProstate-Specific AntigenProstatic NeoplasmsProteomicsBiomarkersBlood ProteinsProstate-Specific Antigen

Identifiers

PMID23763644
PMCPMC3733379

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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.