Evidence map›Paper›PMID 36048090›Full record

ReviewMolecular omics2022

Advancements in automation for plasma proteomics sample preparation.

Christina D King, Kathryn L Kapp, Albert B Arul, Min Ji Choi, Renã A S Robinson

Open access · greenAbstract readReview
In one paragraph

Review in Molecular omics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

8 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. StageTip: a little giant unveiling the potential of mass spectrometry-based proteomics.Analytical sciences : the international journal of the Japan Society for Analytical Chemistry · 2025
    Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Plasma/Serum Proteomics based on Mass Spectrometry.Protein and peptide letters · 2024
    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

5 authors at 1 institution in 1 country.

Christina D KingDepartment of Chemistry, Vanderbilt University, Nashville, Tennessee 37235, USA.
Kathryn L KappDepartment of Chemistry, Vanderbilt University, Nashville, Tennessee 37235, USA.ORCID 0000-0002-1468-8569
Albert B ArulDepartment of Chemistry, Vanderbilt University, Nashville, Tennessee 37235, USA.
Min Ji ChoiDepartment of Chemistry, Vanderbilt University, Nashville, Tennessee 37235, USA.
Renã A S RobinsonDepartment of Chemistry, Vanderbilt University, Nashville, Tennessee 37235, USA.ORCID 0000-0001-6307-8671
Vanderbilt University · US

Funding

Chemistry-Biology Interface Training GrantT32GM065086 · NIGMS · VANDERBILT UNIVERSITY · PI BACHMANN, BRIAN O, SULIKOWSKI, GARY ALLEN · 2002 to 2022
$7.0M
Proteomics of Hypertension and Alzheimer's Disease in African AmericansR01AG064950 · NIA · VANDERBILT UNIVERSITY · PI ROBINSON, RENA A. S. · 2019 to 2023
$4.1M
Vanderbilt Interdisciplinary Training Program in Alzheimer's DiseaseT32AG058524 · NIA · VANDERBILT UNIVERSITY · PI ANGELA L. JEFFERSON · 2018 to 2026
$3.5M
Novel Multiplexing Proteomics to Study the Periphery in Alzheimer's DiseaseR01GM117191 · NIGMS · VANDERBILT UNIVERSITY · PI ROBINSON, RENA A. S. · 2016 to 2020
$2.1M
NIA NIH HHS R01 AG064950NIA NIH HHS T32 AG058524NIGMS NIH HHS R01 GM117191NIGMS NIH HHS T32 GM065086
6 · The paper itself

Abstract

Automation is necessary to increase sample processing throughput for large-scale clinical analyses. Replacement of manual pipettes with robotic liquid handler systems is especially helpful in processing blood-based samples, such as plasma and serum. These samples are very heterogenous, and protein expression can vary greatly from sample-to-sample, even for healthy controls. Detection of true biological changes requires that variation from sample preparation steps and downstream analytical detection methods, such as mass spectrometry, remains low. In this mini-review, we discuss plasma proteomics protocols and the benefits of automation towards enabling detection of low abundant proteins and providing low sample error and increased sample throughput. This discussion includes considerations for automation of major sample depletion and/or enrichment strategies for plasma toward mass spectrometry detection.

Indexed as

ProteomicsAutomationMass Spectrometry

Identifiers

PMID36048090
PMCPMC9879274
OpenAlexW4292640716

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.