Kellie John F, Tran John C, Lee Ji Eun, Ahlf Dorothy R, Thomas Haylee M, Ntai Ioanna, Catherman Adam D, Durbin Kenneth R, Zamdborg Leonid, Vellaichamy Adaikkalam, Thomas Paul M, Kelleher Neil L
Technology Development Team, Center for Top Down Proteomics, University of Illinois at Urbana-Champaign, USA.
Mol Biosyst. 2010 Sep;6(9):1532-9. doi: 10.1039/c000896f. Epub 2010 Mar 29.
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.
自上而下质谱法(MS)已成为蛋白质分析中常见自下而上策略的一种替代方法。在自上而下的方法中,完整的蛋白质在质谱仪中直接裂解,以实现蛋白质鉴定和表征,甚至能够获取组合式翻译后修饰的信息。就在过去两年中,自上而下质谱法在仪器设备和专用软件方面取得了渐进式进展,同时,复杂混合物中全蛋白的精细分离技术也取得了重大进展,这些分离技术具有高回收率和可重复性,也推动了自上而下质谱法的发展。结合不断进步的商用质谱仪器和数据处理技术,在不久的将来,直接可见一个涵盖完整蛋白质和高达70 kDa多肽的高通量工作流程。