Evidence map›Paper›PMID 35842862›Full record

ArticleMetabolomics : Official journal of the Metabolomic Society2022

Prioritize biologically relevant ions for data-independent acquisition (BRI-DIA) in LC-MS/MS-based lipidomics analysis.

Likun Duan, Grace Scheidemantle, Mareca Lodge, Magdalina J Cummings, Eva Pham, Xiaoqiu Wang, Arion Kennedy, Xiaojing Liu

Abstract read
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In one paragraph

Article in Metabolomics : Official journal of the Metabolomic Society, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 29% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Recent Analytical Methodologies in Lipid Analysis.International journal of molecular sciences · 2024
    Review
  6. Article
  7. Myeloid cell MHC I expression drives CD8Frontiers in immunology · 2023
    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

8 authors at 1 institution in 1 country.

Likun Duan *Department of Molecular and Structural Biochemistry, North Carolina State University, Raleigh, NC, 27695, USA.
Grace Scheidemantle *Department of Molecular and Structural Biochemistry, North Carolina State University, Raleigh, NC, 27695, USA.
Mareca LodgeDepartment of Molecular and Structural Biochemistry, North Carolina State University, Raleigh, NC, 27695, USA.
Magdalina J CummingsDepartment of Animal Science, North Carolina State University, Raleigh, NC, 27695, USA.
Eva PhamDepartment of Molecular and Structural Biochemistry, North Carolina State University, Raleigh, NC, 27695, USA.
Xiaoqiu WangDepartment of Animal Science, North Carolina State University, Raleigh, NC, 27695, USA.
Arion KennedyDepartment of Molecular and Structural Biochemistry, North Carolina State University, Raleigh, NC, 27695, USA.
Xiaojing LiuDepartment of Molecular and Structural Biochemistry, North Carolina State University, Raleigh, NC, 27695, USA. xliu68@ncsu.edu.
North Carolina State University · US

Funding

Fructose Induced Regulation of Profibrogenic Factors in Hepatic Nonparenchymal CellsR21DK128678 · NIDDK · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI KENNEDY, ARION · 2021 to 2023
$554k
NIDDK NIH HHS R21 DK128678
6 · The paper itself

Abstract

introductionData-dependent acquisition (DDA) is the most commonly used MS/MS scan method for lipidomics analysis on orbitrap-based instrument. However, MS instrument associated software decide the top N precursors for fragmentation, resulting in stochasticity of precursor selection and compromised consistency and reproducibility. We introduce a novel workflow using biologically relevant lipids to construct inclusion list for data-independent acquisition (DIA), named as BRI-DIA workflow.

objectivesTo ensure consistent coverage of biologically relevant lipids in LC-MS/MS-based lipidomics analysis.

methodsBiologically relevant ion list was constructed based on LIPID MAPS and lipidome atlas in MS-DIAL 4. Lipids were extracted from mouse tissues and used to assess different MS/MS scan workflow (DDA, BRI-DIA, and hybrid mode) on LC-Orbitrap Exploris 480 mass spectrometer.

resultsDDA resulted in more MS/MS events, but the total number of unique lipids identified by three methods (DDA, BRI-DIA, and hybrid MS/MS scan mode) is comparable (580 unique lipids across 44 lipid subclasses in mouse liver). Major cardiolipin molecular species were identified by data generated using BRI-DIA and hybrid methods and allowed calculation of cardiolipin compositions, while identification of the most abundant cardiolipin CL72:8 was missing in data generated using DDA method, leading to wrong calculation of cardiolipin composition.

conclusionThe method of using inclusion list comprised of biologically relevant lipids in DIA MS/MS scan is as efficient as traditional DDA method in profiling lipids, but offers better consistency of lipid identification, compared to DDA method. This study was performed using Orbitrap Exploris 480, and we will further evaluate this workflow on other platforms, and if verified by future work, this biologically relevant ion fragmentation workflow could be routinely used in many studies to improve MS/MS identification capacities.

Indexed as

LipidomicsTandem Mass SpectrometryAnimalsCardiolipinsChromatography, LiquidIonsMetabolomicsMiceReproducibility of ResultsCardiolipinsIons

Identifiers

PMID35842862
OpenAlexW4285677483

What OpenQuestion holds

Textmetadata
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.