AI Article Synopsis

  • Novel LC-MS technologies improve the number of daily runs, but sample preparation has become a challenging bottleneck for throughput.
  • The newly developed positive-pressure 96-well filter-aided sample preparation (PF96) significantly increases throughput by five times while achieving high reproducibility in protein analysis.
  • PF96 is effective for a range of protein loads, and its efficiency, simplicity, and time-saving nature suggest it will be valuable in biomedical and clinical research.

Article Abstract

As novel liquid chromatography-mass spectrometry (LC-MS) technologies for proteomics offer a substantial increase in LC-MS runs per day, robust and reproducible sample preparation emerges as a new bottleneck for throughput. We introduce a novel strategy for positive-pressure 96-well filter-aided sample preparation (PF96) on a commercial positive-pressure solid-phase extraction device. PF96 allows for a five-fold increase in throughput in conjunction with extraordinary reproducibility with Pearson product-moment correlations on the protein level of = 0.9993, as demonstrated for mouse heart tissue lysate in 40 technical replicates. The targeted quantification of 16 peptides in the presence of stable-isotope-labeled reference peptides confirms that PF96 variance is barely assessable against technical variation from nanoLC-MS instrumentation. We further demonstrate that protein loads of 36-60 μg result in optimal peptide recovery, but lower amounts ≥3 μg can also be processed reproducibly. In summary, the reproducibility, simplicity, and economy of time provide PF96 a promising future in biomedical and clinical research.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8981309PMC
http://dx.doi.org/10.1021/acs.jproteome.1c00706DOI Listing

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