Evidence map›Paper›PMID 39536954›Full record

ArticleMolecular & cellular proteomics : MCP2024

Gradient-Elution Nanoflow Liquid Chromatography Without a Binary Pump: Smoothed Step Gradients Enable Reproducible, Sensitive, and Low-Cost Separations for Single-Cell Proteomics.

Kei G I Webber, Siqi Huang, Hsien-Jung L Lin, Tyler L Hunter, Jeremy Tsang, Dasun Jayatunge, Joshua L Andersen, Ryan T Kelly

Abstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

8 authors.

Kei G I WebberDepartment of Chemistry and Biochemistry, Brigham Young University, Provo, Utah, USA.
Siqi HuangDepartment of Chemistry and Biochemistry, Brigham Young University, Provo, Utah, USA.
Hsien-Jung L LinDepartment of Chemistry and Biochemistry, Brigham Young University, Provo, Utah, USA.
Tyler L HunterDepartment of Chemistry and Biochemistry, Brigham Young University, Provo, Utah, USA.
Jeremy TsangDepartment of Oncological Sciences and Huntsman Cancer Institute, University of Utah School of Medicine, Salt Lake, Utah, USA.
Dasun JayatungeDepartment of Oncological Sciences and Huntsman Cancer Institute, University of Utah School of Medicine, Salt Lake, Utah, USA.
Joshua L AndersenDepartment of Oncological Sciences and Huntsman Cancer Institute, University of Utah School of Medicine, Salt Lake, Utah, USA.
Ryan T KellyDepartment of Chemistry and Biochemistry, Brigham Young University, Provo, Utah, USA. Electronic address: ryan.kelly@byu.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mass spectrometry-based proteome profiling of trace analytes including single cells benefits from liquid chromatography separations operated at low flow rates (e.g., <50 nl/min). However, high-pressure binary pumps needed to achieve such flow rates are not commercially available, and instead require splitting of the gradient flow to achieve low-nanoliter-per-minute flow rates. Gradient flow splitting can waste solvent and lead to flow inconsistencies. To address this, we have developed a method for creating gradients by combining segments of mobile phase having increasing solvent strength together in an open capillary, and then relying on Taylor dispersion to form the desired smooth gradient profile. Our method dramatically reduces costs, as only a single isocratic high-pressure pump is required. Following development of gradient profiles for both 10- and 20-min active gradients, we measured 200 pg injections of HeLa digest using a timsTOF mass spectrometer. Finally, we investigated differences in protein expression between single cells originating from two different colonies of ATG-KO HeLa cells. Thousands of proteins were quantified, and a potential mechanism explaining differential immune responses of these two colonies upon exposure to viral DNA treatment was determined.

Indexed as

ProteomicsSingle-Cell AnalysisChromatography, LiquidHeLa CellsHumansNanotechnologyReproducibility of ResultsautophagyHPLC gradient formationnanoflow liquid chromatographysingle-cell proteomicsstepped gradients

Identifiers

PMID39536954
PMCPMC11667035

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Registered trials

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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.