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

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Fully Automated Workflow for Integrated Sample Digestion and Evotip Loading Enabling High-Throughput Clinical Proteomics. / Kverneland, Anders H.; Harking, Florian; Vej-Nielsen, Joel Mario; Huusfeldt, Magnus; Bekker-Jensen, Dorte B.; Svane, Inge Marie; Bache, Nicolai; Olsen, Jesper V.

In: Molecular & cellular proteomics : MCP, Vol. 23, No. 7, 100790, 2024.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Kverneland, AH, Harking, F, Vej-Nielsen, JM, Huusfeldt, M, Bekker-Jensen, DB, Svane, IM, Bache, N & Olsen, JV 2024, 'Fully Automated Workflow for Integrated Sample Digestion and Evotip Loading Enabling High-Throughput Clinical Proteomics', Molecular & cellular proteomics : MCP, vol. 23, no. 7, 100790. https://doi.org/10.1016/j.mcpro.2024.100790

APA

Kverneland, A. H., Harking, F., Vej-Nielsen, J. M., Huusfeldt, M., Bekker-Jensen, D. B., Svane, I. M., Bache, N., & Olsen, J. V. (2024). Fully Automated Workflow for Integrated Sample Digestion and Evotip Loading Enabling High-Throughput Clinical Proteomics. Molecular & cellular proteomics : MCP, 23(7), [100790]. https://doi.org/10.1016/j.mcpro.2024.100790

Vancouver

Kverneland AH, Harking F, Vej-Nielsen JM, Huusfeldt M, Bekker-Jensen DB, Svane IM et al. Fully Automated Workflow for Integrated Sample Digestion and Evotip Loading Enabling High-Throughput Clinical Proteomics. Molecular & cellular proteomics : MCP. 2024;23(7). 100790. https://doi.org/10.1016/j.mcpro.2024.100790

Author

Kverneland, Anders H. ; Harking, Florian ; Vej-Nielsen, Joel Mario ; Huusfeldt, Magnus ; Bekker-Jensen, Dorte B. ; Svane, Inge Marie ; Bache, Nicolai ; Olsen, Jesper V. / Fully Automated Workflow for Integrated Sample Digestion and Evotip Loading Enabling High-Throughput Clinical Proteomics. In: Molecular & cellular proteomics : MCP. 2024 ; Vol. 23, No. 7.

Bibtex

@article{3d7b6045b2ea43e4b1b9f44ade9d4146,
title = "Fully Automated Workflow for Integrated Sample Digestion and Evotip Loading Enabling High-Throughput Clinical Proteomics",
abstract = "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.",
author = "Kverneland, {Anders H.} and Florian Harking and Vej-Nielsen, {Joel Mario} and Magnus Huusfeldt and Bekker-Jensen, {Dorte B.} and Svane, {Inge Marie} and Nicolai Bache and Olsen, {Jesper V.}",
note = "Copyright {\textcopyright} 2024 The Authors. Published by Elsevier Inc. All rights reserved.",
year = "2024",
doi = "10.1016/j.mcpro.2024.100790",
language = "English",
volume = "23",
journal = "Molecular and Cellular Proteomics",
issn = "1535-9476",
publisher = "American Society for Biochemistry and Molecular Biology",
number = "7",

}

RIS

TY - JOUR

T1 - Fully Automated Workflow for Integrated Sample Digestion and Evotip Loading Enabling High-Throughput Clinical Proteomics

AU - Kverneland, Anders H.

AU - Harking, Florian

AU - Vej-Nielsen, Joel Mario

AU - Huusfeldt, Magnus

AU - Bekker-Jensen, Dorte B.

AU - Svane, Inge Marie

AU - Bache, Nicolai

AU - Olsen, Jesper V.

N1 - Copyright © 2024 The Authors. Published by Elsevier Inc. All rights reserved.

PY - 2024

Y1 - 2024

N2 - 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.

AB - 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.

U2 - 10.1016/j.mcpro.2024.100790

DO - 10.1016/j.mcpro.2024.100790

M3 - Journal article

C2 - 38777088

VL - 23

JO - Molecular and Cellular Proteomics

JF - Molecular and Cellular Proteomics

SN - 1535-9476

IS - 7

M1 - 100790

ER -

ID: 397723272