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

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 w...

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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.
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Language:English
Published: United States Elsevier Inc 01-07-2024
American Society for Biochemistry and Molecular Biology
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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. [Display omitted] •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.
AbstractList 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. • 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.
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.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.
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. [Display omitted] •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.
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.
ArticleNumber 100790
Author Harking, Florian
Bache, Nicolai
Huusfeldt, Magnus
Kverneland, Anders H.
Olsen, Jesper V.
Svane, Inge Marie
Bekker-Jensen, Dorte B.
Vej-Nielsen, Joel Mario
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  givenname: Florian
  surname: Harking
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  givenname: Joel Mario
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  surname: Vej-Nielsen
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  organization: Evosep Biosystems, Odense, Denmark
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  givenname: Magnus
  surname: Huusfeldt
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  organization: Evosep Biosystems, Odense, Denmark
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  givenname: Inge Marie
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  fullname: Svane, Inge Marie
  organization: Department of Oncology, National Center of Cancer Immune Therapy, Copenhagen University Hospital - Herlev and Gentofte, Herlev, Denmark
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  givenname: Nicolai
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  givenname: Jesper V.
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  surname: Olsen
  fullname: Olsen, Jesper V.
  email: jesper.olsen@cpr.ku.dk
  organization: Faculty of Health Sciences, Novo Nordisk Foundation Center for Protein Research, University of Copenhagen, Copenhagen, Denmark
BackLink https://www.ncbi.nlm.nih.gov/pubmed/38777088$$D View this record in MEDLINE/PubMed
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Issue 7
Keywords 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
Language English
License This is an open access article under the CC BY license.
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These authors contributed equally to this work.
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cancer immune therapy
Collection: Advances in Proteomics Technology
mass spectrometry
plasma proteomics
workflow automation
Title Fully Automated Workflow for Integrated Sample Digestion and Evotip Loading Enabling High-Throughput Clinical Proteomics
URI https://dx.doi.org/10.1016/j.mcpro.2024.100790
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