Evidence map›Paper›PMID 40989151›Full record

ArticleBMC methods2025

A cross-species proteomic assessment of cost-effective platforms for depleting high-abundant proteins from blood serum.

Zongkai Peng, Shakya Wije Munige, Deepti Bhusal, Isabella L Yang, Zhibo Yang, Nagib Ahsan

Abstract read
In one paragraph

Article in BMC methods, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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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

6 authors.

Zongkai Peng *Department of Chemistry and Biochemistry, University of Oklahoma, Norman, OK 73019 USA.
Shakya Wije Munige *Department of Chemistry and Biochemistry, University of Oklahoma, Norman, OK 73019 USA.
Deepti Bhusal *Department of Chemistry and Biochemistry, University of Oklahoma, Norman, OK 73019 USA.
Isabella L YangDepartment of Psychology, University of Oklahoma, Norman, OK 73019 USA.
Zhibo YangDepartment of Chemistry and Biochemistry, University of Oklahoma, Norman, OK 73019 USA.
Nagib AhsanDepartment of Chemistry and Biochemistry, University of Oklahoma, Norman, OK 73019 USA.

Funding

Novel single-cell mass spectrometry methods to assess the role of intracellular drug concentration and metabolism in antimicrobial treatment failureR01AI177469 · NIAID · UNIVERSITY OF OKLAHOMA · PI Laura-Isobel McCall, Zhibo Yang · 2023 to 2026
$1.6M
NIAID NIH HHS R01 AI177469
6 · The paper itself

Abstract

Background: Blood proteome analysis is becoming increasingly popular in veterinary research because many animal models have been used to study a range of human diseases. Most of the commercial high-abundance protein (HAP) depletion kits are optimized for human serum, whereas proteins in animal serum may not be present in human serum or may be present at different abundances. There are no previous studies investigating the efficacy of using various HAP kits for proteome analysis of animal serums. Method: We used three commercial serum abundant protein depletion (SAPD) kits (i.e., ion exchange-based Norgen kit (ProteoSpin™), antibody-based Thermo Albumin Depletion Kit (Pierce™), solubility-based kit (Minute™), and a cost-effective method (i.e., perchloric acid (PerCA) HAP precipitation) to assess their effectiveness to process serums from five different species (i.e., mouse, chicken, dog, goat, and guinea pig). Protocols of the commercial kits were adopted from manufacturers' guidelines with minor modifications for optimized performance. Following HAP depletion, proteins from all species were digested using a Trypsin/Lys-C enzyme mix, desalted, and subjected to label-free quantitative bottom-up proteomics analysis via liquid chromatography-tandem mass spectrometry (LC-MS/MS). The raw data were processed using the Andromeda search engine integrated into MaxQuant, and peptide identification was performed by searching against the UniProt-reviewed protein database. Advanced bioinformatics tools were employed to facilitate data analysis and visualization, ensuring comprehensive interpretation of the depletion efficiency and comparative performance of the methods across species. Result: We determined their capabilities of protein identification (Norgen kit > Minute kit > PerCA precipitation > Thermo kit), depletion efficiencies of HAPs (Minute kit > Norgen kit > PerCA precipitation > Thermo kit), and cost-effectiveness (PerCA precipitation > Minute kit > Norgen kit > Thermo kit). Our results show that the PerCA precipitation method, which is > 20 times cheaper than commercial kits, outperforms other methods in depleting HAPs, especially in mouse serum. While Norgen kit excels in mouse and goat serum, the PerCA precipitation method offers broader applicability and reveals unique low abundant proteins. Protein pathway analysis highlights distinct biological processes affected by different depletion methods. Discussion: Overall, our studies provide valuable insights into protein depletion techniques, with the PerCA depletion method emerging as a cost-effective and versatile option for proteomics research across various serums.

Indexed as

Cross speciesDepletion methodsHigh abundance proteinProteomics

Identifiers

PMID40989151
PMCPMC12450807

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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.