| Literature DB >> 20711533 |
John F Kellie1, John C Tran, Ji Eun Lee, Dorothy R Ahlf, Haylee M Thomas, Ioanna Ntai, Adam D Catherman, Kenneth R Durbin, Leonid Zamdborg, Adaikkalam Vellaichamy, Paul M Thomas, Neil L Kelleher.
Abstract
Top Down mass spectrometry (MS) has emerged as an alternative to common Bottom Up strategies for protein analysis. In the Top Down approach, intact proteins are fragmented directly in the mass spectrometer to achieve both protein identification and characterization, even capturing information on combinatorial post-translational modifications. Just in the past two years, Top Down MS has seen incremental advances in instrumentation and dedicated software, and has also experienced a major boost from refined separations of whole proteins in complex mixtures that have both high recovery and reproducibility. Combined with steadily advancing commercial MS instrumentation and data processing, a high-throughput workflow covering intact proteins and polypeptides up to 70 kDa is directly visible in the near future.Entities:
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Year: 2010 PMID: 20711533 PMCID: PMC3115741 DOI: 10.1039/c000896f
Source DB: PubMed Journal: Mol Biosyst ISSN: 1742-2051