Evidence map›Paper›PMID 39088833›Full record

ReviewProteomics2025

Data acquisition approaches for single cell proteomics.

Gautam Ghosh, Ariana E Shannon, Brian C Searle

Abstract readReview
In one paragraph

Review in Proteomics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Classification with Missing Data - AbioRxiv : the preprint server for biology · 2026
    Article
  5. Article
  6. Article
  7. Review
  8. Slice-PASEF: Maximising Ion Utilisation in LC-MS Proteomics.bioRxiv : the preprint server for biology · 2025
    Article
  9. 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

3 authors.

Gautam GhoshOhio State Biochemistry Program, The Ohio State University, Columbus, Ohio, USA.
Ariana E ShannonPelotonia Institute for Immuno-Oncology, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio, USA.
Brian C SearleOhio State Biochemistry Program, The Ohio State University, Columbus, Ohio, USA.ORCID 0000-0001-8760-6731

Funding

Investigating the functional impact of genetic variants in the human proteomeR35GM150723 · NIGMS · OHIO STATE UNIVERSITY · PI Brian Chih-Seng Searle · 2023 to 2026
$1.6M
Using proteogenomics to assess the functional impact of alternative splicing events in glioblastomaR21CA267394 · NCI · SWEDISH MEDICAL CENTER, FIRST HILL · PI COBBS, CHARLES S, SEARLE, BRIAN CHIH-SENG · 2023 to 2024
$426k
NCI NIH HHS R21 CA267394NIGMS NIH HHS R35 GM150723NIH HHS R21CA267394NIH HHS R35GM150723
6 · The paper itself

Abstract

Single-cell proteomics (SCP) aims to characterize the proteome of individual cells, providing insights into complex biological systems. It reveals subtle differences in distinct cellular populations that bulk proteome analysis may overlook, which is essential for understanding disease mechanisms and developing targeted therapies. Mass spectrometry (MS) methods in SCP allow the identification and quantification of thousands of proteins from individual cells. Two major challenges in SCP are the limited material in single-cell samples necessitating highly sensitive analytical techniques and the efficient processing of samples, as each biological sample requires thousands of single cell measurements. This review discusses MS advancements to mitigate these challenges using data-dependent acquisition (DDA) and data-independent acquisition (DIA). Additionally, we examine the use of short liquid chromatography gradients and sample multiplexing methods that increase the sample throughput and scalability of SCP experiments. We believe these methods will pave the way for improving our understanding of cellular heterogeneity and its implications for systems biology.

Indexed as

ProteomeProteomicsSingle-Cell AnalysisAnimalsChromatography, LiquidHumansMass SpectrometryProteomedata dependent acquisitiondata independent acquisitionmass spectrometrymultiplexproteomicssingle cell

Identifiers

PMID39088833
PMCPMC11735665

What OpenQuestion holds

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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.