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February 19, 2026Journal of Proteome Research0 citationsOpen Access

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

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GRGeorgia RoumeliotiAMAlex MontoyaGFGemma Fisher

Key Points

  • This research aims to improve sample preparation efficiency in high-throughput proteomics workflows, particularly for PTM profiling.
  • Utilized Gilson Platemaster P220 pipettor and VP Scientific 96-well magnetic pin device for sample processing.
  • Achieved phosphoproteomics workflows in 96-well format with minimized operator workload.
  • Developed cost-efficient 96-well solid-phase extraction plates for improved sample processing.
  • Characterized loading capacity and lipid removal efficiency of the solid-phase extraction plates.
  • Completed PAC/SP3 digestion, desalting, phosphopeptide enrichment, and second desalting within 2 days.
  • Eliminated the need for continuous bead suspension during digestion, simplifying the workflow.
  • Demonstrated that the method minimizes operator variability and improves reproducibility.

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.

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Cite This Study

Roumelioti et al. (2026) studied this question.

synapsesocial.com/papers/6996a798ecb39a600b3ed576https://doi.org/10.1021/acs.jproteome.5c01020
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