Ilgisonis Ekaterina V, Pogodin Pavel V, Kiseleva Olga I, Tarbeeva Svetlana N, Ponomarenko Elena A
Institute of Biomedical Chemistry, Pogodinskaya Street, 10, 119121 Moscow, Russia.
J Pers Med. 2022 Mar 16;12(3):479. doi: 10.3390/jpm12030479.
Within the Human Proteome Project initiative framework for creating functional annotations of uPE1 proteins, the neXt-CP50 Challenge was launched in 2018. In analogy with the missing-protein challenge, each command deciphers the functional features of the proteins in the chromosome-centric mode. However, the neXt-CP50 Challenge is more complicated than the missing-protein challenge: the approaches and methods for solving the problem are clear, but neither the concept of protein function nor specific experimental and/or bioinformatics protocols have been standardized to address it. We proposed using a retrospective analysis of the key HPP repository, the neXtProt database, to identify the most frequently used experimental and bioinformatic methods for analyzing protein functions, and the dynamics of accumulation of functional annotations. It has been shown that the dynamics of the increase in the number of proteins with known functions are greater than the progress made in the experimental confirmation of the existence of questionable proteins in the framework of the missing-protein challenge. At the same time, the functional annotation is based on the guilty-by-association postulate, according to which, based on large-scale experiments on API-MS and Y2H, proteins with unknown functions are most likely mapped through "handshakes" to biochemical processes.
在人类蛋白质组计划创建uPE1蛋白质功能注释的倡议框架内,2018年发起了neXt-CP50挑战。与缺失蛋白质挑战类似,每个指令都以染色体为中心的模式解读蛋白质的功能特征。然而,neXt-CP50挑战比缺失蛋白质挑战更为复杂:解决问题的方法和手段是明确的,但蛋白质功能的概念以及用于解决该问题的具体实验和/或生物信息学协议都尚未标准化。我们建议对关键的HPP知识库(即neXtProt数据库)进行回顾性分析,以确定分析蛋白质功能最常用的实验和生物信息学方法,以及功能注释的积累动态。结果表明,已知功能蛋白质数量增加的动态大于在缺失蛋白质挑战框架内对可疑蛋白质存在进行实验确认所取得的进展。同时,功能注释基于关联有罪假设,根据该假设,基于API-MS和Y2H的大规模实验,功能未知的蛋白质最有可能通过“握手”映射到生化过程。