Evidence map›Paper›PMID 37167627›Full record

ArticleAnalytical chemistry2023

HyperSCP: Combining Isotopic and Isobaric Labeling for Higher Throughput Single-Cell Proteomics.

Yiran Liang, Thy Truong, Aubrianna J Saxton, Hannah Boekweg, Samuel H Payne, Pam M Van Ry, Ryan T Kelly

Abstract read
In one paragraph

Article in Analytical chemistry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Plasma-Derived Extracellular Vesicle Proteomics.Journal of proteome research · 2025
    Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. What's new in single-cell proteomics.Current opinion in biotechnology · 2024
    Review
  18. Article
  19. Article
  20. Article
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

7 authors.

Yiran LiangDepartment of Chemistry and Biochemistry, Brigham Young University, Provo, Utah 84602, United States.
Thy TruongDepartment of Chemistry and Biochemistry, Brigham Young University, Provo, Utah 84602, United States.
Aubrianna J SaxtonDepartment of Chemistry and Biochemistry, Brigham Young University, Provo, Utah 84602, United States.ORCID 0000-0002-9466-7900
Hannah BoekwegDepartment of Biology, Brigham Young University, Provo, Utah 84602, United States.
Samuel H PayneDepartment of Biology, Brigham Young University, Provo, Utah 84602, United States.ORCID 0000-0002-8351-1994
Pam M Van RyDepartment of Chemistry and Biochemistry, Brigham Young University, Provo, Utah 84602, United States.ORCID 0000-0003-0195-7229
Ryan T KellyDepartment of Chemistry and Biochemistry, Brigham Young University, Provo, Utah 84602, United States.ORCID 0000-0002-3339-4443

Funding

Fully automated and ultra-high-throughput platform for in-depth single-cell proteomicsR01GM138931 · NIGMS · BRIGHAM YOUNG UNIVERSITY · PI KELLY, RYAN T · 2020 to 2023
$1.6M
NIGMS NIH HHS R01 GM138931
6 · The paper itself

Abstract

Recent developments in mass spectrometry-based single-cell proteomics (SCP) have resulted in dramatically improved sensitivity, yet the relatively low measurement throughput remains a limitation. Isobaric and isotopic labeling methods have been separately applied to SCP to increase throughput through multiplexing. Here we combined both forms of labeling to achieve multiplicative scaling for higher throughput. Two-plex stable isotope labeling of amino acids in cell culture (SILAC) and isobaric tandem mass tag (TMT) labeling enabled up to 28 single cells to be analyzed in a single liquid chromatography-mass spectrometry (LC-MS) analysis, in addition to carrier, reference, and negative control channels. A custom nested nanowell chip was used for nanoliter sample processing to minimize sample losses. Using a 145-min total LC-MS cycle time, ∼280 single cells were analyzed per day. This measurement throughput could be increased to ∼700 samples per day with a high-duty-cycle multicolumn LC system producing the same active gradient. The labeling efficiency and achievable proteome coverage were characterized for multiple analysis conditions.

Indexed as

ProteomicsTandem Mass SpectrometryChromatography, LiquidIsotope LabelingProteomeProteome

Identifiers

PMID37167627
PMCPMC10246935

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.