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The chromosome-centric human proteome project at FEBS congress

机译:FEBS大会上以染色体为中心的人类蛋白质组计划

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摘要

In the summer of 2013, distinguished global representatives of proteome science gathered to discuss the futuristic visions of the chromosome-centric human proteome project (C-HPP) (Cochairs: Y. K. Paik, G. Omenn; hosted by A. Archakov, Institute of Biomedical Chemistry, Russia) that was broadcast to the annual Federation of European Biochemical Societies Congress (St. Petersburg, Russia, July 10-11, 2013). Technology breakthroughs presented included a new ultra-sensitive Tribrid mass-spectrometer from Thermo and SOMAmers-Slow Off-rate Modified Aptamers (SOMAlogic, USA), a new type of protein capture reagents. Professor Archakov's group introduced the "rectangle" concept of proteome size as a product of proteome width and depth. The discussion on proteome width culminated with the introduction of digital biomarkers-low-copied aberrant proteins that differ from their typical forms by PTMs, alternative splicing, or single amino acid polymorphisms. The aberrant proteoforms, a complement to whole-genome proteomic surveys, were presented as an ultimate goal for the proteomic community.
机译:2013年夏天,蛋白质组学的全球杰出代表聚集一堂,讨论以染色体为中心的人类蛋白质组计划(C-HPP)的未来愿景(共同主席:YK Paik,G. Omenn;由生物医学研究所的A. Archakov主持)每年的欧洲生物化学协会联合会(2013年7月10日至11日,俄罗斯圣彼得堡)播放。展示的技术突破包括新型的蛋白质捕获试剂,来自Thermo和SOMAmers的新型超灵敏三重质谱仪-慢减量速率修饰的适体(SOMAlogic,美国)。 Archakov教授的小组介绍了蛋白质组大小的“矩形”概念,将其作为蛋白质组宽度和深度的乘积。关于蛋白质组宽度的讨论最终以引入数字生物标记物-低复制异常蛋白而告终,这些蛋白与PTM,替代剪接或单氨基酸多态性的典型形式不同。作为全基因组蛋白质组学调查的补充,异常蛋白质组是蛋白质组学的最终目标。

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