Journal
JOURNAL OF PROTEOME RESEARCH
Volume 20, Issue 3, Pages 1676-1688Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.jproteome.0c00890
Keywords
sample preparation; on-membrane digestion; micro-SPE tip; limited samples; label-free quantitation; bottom-up nanoLC-MS-based proteomics; OmSET (on-microsolid-phase extraction tip)
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Funding
- NIH [R01GM120272, R01CA218500, R35GM136421]
- DanaFarber Cancer Institute/Northeastern University Joint Program in Cancer Drug Development Award
- Thermo Fisher Scientific through a Technology Alliance Partnership program
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The developed OmSET method is efficient and reproducible for processing limited biological samples, with minimal sample volumes and all processing steps conducted on-membrane in a single microreactor. It has been shown to provide reliable label-free quantitation results for low numbers of human monocytes, with excellent correlations between protein abundances and the amounts of starting material, as well as between sample processing replicates.
In-depth LC-MS-based proteomic profiling of limited biological and clinical samples, such as rare cells or tissue sections from laser capture microdissection or microneedle biopsies, has been problematic due, in large, to the inefficiency of sample preparation and attendant sample losses. To address this issue, we developed on-microsolid-phase extraction tip (OmSET)-based sample preparation for limited biological samples. OmSET is simple, efficient, reproducible, and scalable and is a widely accessible method for processing similar to 200 to 10,000 cells. The developed method benefits from minimal sample processing volumes (1-3 mu L) and conducting all sample processing steps on-membrane within a single microreactor. We first assessed the feasibility of using micro-SPE tips for nanogram-level amounts of tryptic peptides, minimized the number of required sample handling steps, and reduced the hands-on time. We then evaluated the capability of OmSET for quantitative analysis of low numbers of human monocytes. Reliable and reproducible label-free quantitation results were obtained with excellent correlations between protein abundances and the amounts of starting material (R-2 = 0.93) and pairwise correlations between sample processing replicates (R-2 = 0.95) along with the identification of approximately 300, 1800, and 2000 protein groups from injected similar to 10, 100, and 500 cell equivalents, resulting from processing approximately 200, 2000, and 10,000 cells, respectively.
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