High-Throughput Proteomics Sample Preparation Using a 96-Channel Pipettor and Magnetic Pin Device

High-throughput proteomics requires efficient and highly reproducible sample processing, yet workflows─particularly for PTM profiling─remain complex and costly to fully automate. Here, we present a practical intermediate solution using manually operated 96-channel devices: the Gilson Platemaster P220 pipettor and VP Scientific 96-well magnetic pin device. Using this setup, we achieved robust and reproducible phosphoproteomics in a 96-well format, completing protein aggregation capture (PAC/SP3) digestion, desalting, phosphopeptide enrichment, and a second desalting step within 2 days while minimizing operator workload and variability. Several innovations enable this workflow. First, we describe a cost-efficient method to generate 96-well solid-phase extraction plates by directly packing the Oasis HLB sorbent into tapered filter plates. We extensively characterize these plates in terms of loading capacity, lipid removal efficiency, and suitability for high-pH fractionation. Second, we demonstrate that efficient PAC digestion does not require continuous bead suspension; instead, digestion can be achieved by briefly aspirating beads in protease solution, eliminating the need for orbital shaking and simplifying automation. The presented workflow familiarizes users with 96-channel devices and hence serves as a good step toward full automation.

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Publication Details

Journal
Journal of Proteome Research
Published
2026-02-16
DOI
https://doi.org/10.1021/acs.jproteome.5c01020
Primary Topic
Advanced Proteomics Techniques and Applications
Type
article
Field-Weighted Citation Impact
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article

High-Throughput Proteomics Sample Preparation Using a 96-Channel Pipettor and Magnetic Pin Device

Pavel V. Shliaha, David Carling, Jesús Gil, Christian Speck et al.
Journal of Proteome Research
Advanced Proteomics Techniques and Applications
article

High-Throughput Proteomics Sample Preparation Using a 96-Channel Pipettor and Magnetic Pin Device

Pavel V. Shliaha, David Carling, Jesús Gil, Christian Speck, Luís Aragón, Oleh Lushchak, Gemma Fisher, Emma Lara Navarro, Santiago Vernia, Aleksandra Gruevska, Louise Fets, Alexis R. Barr, Luc-Alban Vuillemenot, Alex Montoya, Georgia Roumelioti, Sijia Yu, Oliver Gonzalez-Carvajal, Elizabeth Pyman, Naveenan Navaratnam, Jodie Birch, Jane Bennett, Zoe Hall, Angela Woods
article en

Abstract

High-throughput proteomics requires efficient and highly reproducible sample processing, yet workflows─particularly for PTM profiling─remain complex and costly to fully automate. Here, we present a practical intermediate solution using manually operated 96-channel devices: the Gilson Platemaster P220 pipettor and VP Scientific 96-well magnetic pin device. Using this setup, we achieved robust and reproducible phosphoproteomics in a 96-well format, completing protein aggregation capture (PAC/SP3) digestion, desalting, phosphopeptide enrichment, and a second desalting step within 2 days while minimizing operator workload and variability. Several innovations enable this workflow. First, we describe a cost-efficient method to generate 96-well solid-phase extraction plates by directly packing the Oasis HLB sorbent into tapered filter plates. We extensively characterize these plates in terms of loading capacity, lipid removal efficiency, and suitability for high-pH fractionation. Second, we demonstrate that efficient PAC digestion does not require continuous bead suspension; instead, digestion can be achieved by briefly aspirating beads in protease solution, eliminating the need for orbital shaking and simplifying automation. The presented workflow familiarizes users with 96-channel devices and hence serves as a good step toward full automation.

Journal of Proteome ResearchVol. 25(3)
Kyiv School of Economics (UA), Hammersmith Hospital (GB), National University (US), Instituto de Biomedicina de Valencia (ES), Centro de Investigacion Principe Felipe (ES)
Openalex Percentile: Top 56%
Advanced Proteomics Techniques and Applications
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