An EasyPep Magnetic Solution for Automated Proteomics Sample Preparation
Posters | 2024 | Thermo Fisher Scientific | ASMSInstrumentation
Magnetic bead–based sample preparation has emerged as a critical approach in proteomics, enabling streamlined protein cleanup, high reproducibility, and compatibility with automation. By replacing laborious centrifugation and SpeedVac steps, magnetic workflows accelerate sample throughput and minimize variability, meeting the growing demand for large-scale, high-quality proteomic analyses in research and clinical environments.
This study introduces the EasyPep Magnetic MS Sample Prep Kit and evaluates its performance across diverse sample types, automation platforms, and analytical instruments. Key objectives include:
The EasyPep Magnetic workflow integrates preformulated buffers, MS-grade enzyme mix, and proprietary magnetic beads. Samples (1 µg–1.5 mg) undergo reduction, alkylation, digestion, and bead-based peptide cleanup, with eluted peptides ready for direct LC-MS analysis. Instrumentation included:
Performance benchmarks demonstrated:
The EasyPep Magnetic solution offers:
Advancements in magnetic bead chemistries and automation will further reduce hands-on time and broaden sample compatibility (e.g., single-cell proteomics, cross-linking studies). Integration with emerging high-resolution instruments and AI-driven data analysis promises deeper proteome coverage, faster turnaround, and robust biomarker validation in translational research.
The EasyPep Magnetic MS Sample Prep Kit delivers a streamlined, reliable, and high-throughput solution for proteomic sample preparation. Its versatile compatibility, automation readiness, and reproducible performance position it as an effective tool for diverse proteomic workflows, from basic research to clinical applications.
1. Hughes CS, Moggridge S, Müller T et al. Single-pot, solid-phase-enhanced sample preparation for proteomics experiments. Nat Protoc. 2019;14(1):68–85.
2. Waas M, Pereckas M, Jones-Lipinski RA, Ashwood C, Gundry RL. SP2: Rapid and automatable contaminant removal from peptide samples for proteomic analyses. J Proteome Res. 2019;18(4):1644–1656.
Sample Preparation
IndustriesProteomics
ManufacturerThermo Fisher Scientific
Summary
Importance of the Topic
Magnetic bead–based sample preparation has emerged as a critical approach in proteomics, enabling streamlined protein cleanup, high reproducibility, and compatibility with automation. By replacing laborious centrifugation and SpeedVac steps, magnetic workflows accelerate sample throughput and minimize variability, meeting the growing demand for large-scale, high-quality proteomic analyses in research and clinical environments.
Goals and Study Overview
This study introduces the EasyPep Magnetic MS Sample Prep Kit and evaluates its performance across diverse sample types, automation platforms, and analytical instruments. Key objectives include:
- Demonstrate compatibility with mammalian cells, plasma, tissue, and bacteria.
- Benchmark digestion efficiency, peptide/protein identification yield, and quantification precision.
- Validate automated processing on KingFisher and Hamilton systems, including high-throughput applications.
Methodology and Instrumentation
The EasyPep Magnetic workflow integrates preformulated buffers, MS-grade enzyme mix, and proprietary magnetic beads. Samples (1 µg–1.5 mg) undergo reduction, alkylation, digestion, and bead-based peptide cleanup, with eluted peptides ready for direct LC-MS analysis. Instrumentation included:
- Automated platforms: Thermo Scientific KingFisher Apex, Hamilton Apex.
- LC systems: Vanquish Neo UPLC, Dionex Ultimate 3000 Nano LC.
- Columns: EASY-Spray PepMap Neo (75 µm × 50 cm).
- Mass spectrometers: Orbitrap Exploris 480 (DIA), Orbitrap Astral (DIA), Q Exactive Plus (DDA, TMT/TMTpro).
- Data analysis software: Proteome Discoverer 3.0/3.1, Spectronaut 18, CHIMERYS.
Main Results and Discussion
Performance benchmarks demonstrated:
- Comparable peptide and protein identifications to established workflows (SP3, AccelerOme) with >60 000 peptides and >5 900 proteins from 25 µg HeLa lysate.
- High digestion efficiency (>88% zero missed cleavages) and quantification reproducibility (median CV <10%).
- Robust peptide yield (∼47% recovery) and low variability (<10% CV) across 96 plasma samples, including NSCLC vs normal donors.
- Successful processing of FFPE colon tumor/normal tissues, identifying ∼3 700 proteins with 94% overlap and detecting known biomarkers (HPGD downregulation, CEACAM6 upregulation).
Benefits and Practical Applications
The EasyPep Magnetic solution offers:
- Rapid end-to-end sample preparation (<3 hours) without centrifugation or vacuum concentration.
- Scalability from microgram to milligram inputs and compatibility with multiplexed quantification (TMT/TMTpro).
- Seamless integration into existing automation platforms for high-throughput studies, supporting up to 60 LC-MS injections per day.
- Enhanced laboratory productivity and consistent data quality for QA/QC, biomarker discovery, and clinical proteomics.
Future Trends and Opportunities
Advancements in magnetic bead chemistries and automation will further reduce hands-on time and broaden sample compatibility (e.g., single-cell proteomics, cross-linking studies). Integration with emerging high-resolution instruments and AI-driven data analysis promises deeper proteome coverage, faster turnaround, and robust biomarker validation in translational research.
Conclusion
The EasyPep Magnetic MS Sample Prep Kit delivers a streamlined, reliable, and high-throughput solution for proteomic sample preparation. Its versatile compatibility, automation readiness, and reproducible performance position it as an effective tool for diverse proteomic workflows, from basic research to clinical applications.
References
1. Hughes CS, Moggridge S, Müller T et al. Single-pot, solid-phase-enhanced sample preparation for proteomics experiments. Nat Protoc. 2019;14(1):68–85.
2. Waas M, Pereckas M, Jones-Lipinski RA, Ashwood C, Gundry RL. SP2: Rapid and automatable contaminant removal from peptide samples for proteomic analyses. J Proteome Res. 2019;18(4):1644–1656.
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