Fully Automated Workflow for Integrated Sample Digestion and Evotip Loading Enabling High-Throughput Clinical Proteomics

• Published in: Molecular & cellular proteomics Vol. 23; no. 7; p. 100790
• Main Authors: Kverneland, Anders H., Harking, Florian, Vej-Nielsen, Joel Mario, Huusfeldt, Magnus, Bekker-Jensen, Dorte B., Svane, Inge Marie, Bache, Nicolai, Olsen, Jesper V.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01-07-2024; American Society for Biochemistry and Molecular Biology
• Subjects: biomarker discovery; cancer immune therapy; Collection: Advances in Proteomics Technology; mass spectrometry; plasma proteomics; workflow automation; BCA; cancer immune therapy; CAA; RT; JNK; MS; SPD; HCD; PTM; Ti-IMAC; ACN; biomarker discovery; plasma proteomics; PAC; workflow automation; LC; mass spectrometry; AGC; DIA; TCEP
• ISSN: 1535-9476; 1535-9484; 1535-9484
• DOI: 10.1016/j.mcpro.2024.100790

Protein identification and quantification is an important tool for biomarker discovery. With the increased sensitivity and speed of modern mass spectrometers, sample preparation remains a bottleneck for studying large cohorts. To address this issue, we prepared and evaluated a simple and efficient workflow on the Opentrons OT-2 robot that combines sample digestion, cleanup, and loading on Evotips in a fully automated manner, allowing the processing of up to 192 samples in 6 h. Analysis of 192 automated HeLa cell sample preparations consistently identified ∼8000 protein groups and ∼130,000 peptide precursors with an 11.5 min active liquid chromatography gradient with the Evosep One and narrow-window data-independent acquisition (nDIA) with the Orbitrap Astral mass spectrometer providing a throughput of 100 samples per day. Our results demonstrate a highly sensitive workflow yielding both reproducibility and stability at low sample inputs. The workflow is optimized for minimal sample starting amount to reduce the costs for reagents needed for sample preparation, which is critical when analyzing large biological cohorts. Building on the digesting workflow, we incorporated an automated phosphopeptide enrichment step using magnetic titanium-immobilized metal ion affinity chromatography beads. This allows for a fully automated proteome and phosphoproteome sample preparation in a single step with high sensitivity. Using the integrated digestion and Evotip loading workflow, we evaluated the effects of cancer immune therapy on the plasma proteome in metastatic melanoma patients.
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•Automated sample prep for LC-MS proteomics for up 192 samples in less than 7 h.•Integration of digestion and Evotip loading reduces sample input and reagents needed.•More than 120k quantified peptides in HeLa cells from 1 μg protein on 12 min gradients.•The workflow can be expanded to include phosphopeptide enrichment.
The throughput of shotgun proteomics has been increased significantly and opened up for analysis of large clinical cohorts. Automation of the sample preparation step is highly desirable for robust and cost-effective proteomics and phosphoproteomics analyses. In this manuscript, we show that fully automated proteomics sample preparation is easily achievable with the Opentrons OT2 robot preparing up to 192 samples in parallel with only minimal handling time. We demonstrate the potential of this workflow in a clinical cohort of plasma samples.