Brief Evaluation of Olink Reveal Proximity Extension Assay for High-Throughput Proteomics: A Case Study Using NIST SRM 1950 and Two Spike-In Protein Standards
Yuri E. M. van der Burgt, , , Emile de Meijer, , and , Magnus Palmblad*,
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引用次数: 0
Abstract
Plasma proteomics has regained attention in recent years through advancements in mass spectrometry instrumentation and sample preparation as well as new high-throughput affinity-based technologies. Here, we evaluate the analytical performance of the new Olink Reveal platform, a proximity extension assay (PEA)-based technology quantifying 1034 proteins and covering many biological pathways, in particular immune system processes. Using spiked-in recombinant Interleukin-10 (IL-10) and vascular endothelial growth factor D (VEGF-D) in the NIST SRM 1950 plasma standard, we assessed the linearity, sensitivity, precision, and accuracy of the Olink Reveal assay. The results demonstrated strong linear relationships (R2 0.922–0.953) for both IL-10 and VEGF-D across spiked-in concentrations, confirming the robust technical performance for these two proteins in the Olink Reveal platform. The resulting data contain no sensitive or personally identifiable information and are therefore suitable for use in benchmarking and software development. The data are publicly available in the PRIDE repository with identifier PAD000009.
期刊介绍:
Journal of Proteome Research publishes content encompassing all aspects of global protein analysis and function, including the dynamic aspects of genomics, spatio-temporal proteomics, metabonomics and metabolomics, clinical and agricultural proteomics, as well as advances in methodology including bioinformatics. The theme and emphasis is on a multidisciplinary approach to the life sciences through the synergy between the different types of "omics".