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pmid:39127789

Comprehensive immune cell spectral library for large-scale human primary T, B, and NK cell proteomics.

Hyeon-Jeong Lee · Yoondam Seo · Yoon Park · Eugene C Yi · Dohyun Han · Hophil Min

Scientific data · 2024 doi:10.1038/s41597-024-03721-2

Paper

complete

Experiment

partial

Data

partial

Analysis

partial

Execution

absent

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Comprehensive immune cell spectral library for large-scale human primary T, B, and NK cell proteomics.
doi
10.1038/s41597-024-03721-2
pmid
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Hyeon-Jeong Lee
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Yoondam Seo
[2]
Yoon Park
[3]
Eugene C Yi
[4]
Dohyun Han
[5]
Hophil Min
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Scientific data
year
2024
abstract
Although proteomics is extensively used in immune research, there is currently no publicly accessible spectral assay library for the comprehensive proteome of immune cells. This study generated spectral assay libraries for five human immune cell lines and four primary immune cells: CD4 T, CD8 T, natural killer (NK) cells, and B cells. This was achieved by utilizing data-dependent acquisition (DDA) and employing fractionated samples from over 100 µg of proteins, which was applied to acquire the highest-quality MS/MS spectral data. In addition, Data-indedendent acquisition (DIA) was used to obtain sufficient data points for analyzing proteins from 10,000 primary CD4 T, CD8 T, NK, and B cells. The immune cell spectral assay library generated included 10,544 protein groups and 127,106 peptides. The proteomic profiles of 10,000 primary human immune cells obtained from 15 healthy volunteers analyzed using DIA revealed the highest heterogeneity of B cells among other immune cell types and the similarity between CD4 T and CD8 T cells. All data and spectral library are deposited in ProteomeXchange (PXD047742).
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As a result, 682 proteins were evaluated for their different profiles among the four types of immune cells; among them, expression levels of representative proteins were visualized with violin plots in Fig. 5.
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