Suppr超能文献

17 号染色体缺失蛋白:作为 neXt-MP50 挑战的一部分的最新进展和未来方向。

Chromosome 17 Missing Proteins: Recent Progress and Future Directions as Part of the neXt-MP50 Challenge.

机构信息

Department of Electronic Engineering and Computer Science , University of Michigan , Ann Arbor , Michigan 48109 , United States.

Department of Computational Medicine and Bioinformatics , University of Michigan , Ann Arbor , Michigan 48109 , United States.

出版信息

J Proteome Res. 2018 Dec 7;17(12):4061-4071. doi: 10.1021/acs.jproteome.8b00442. Epub 2018 Oct 23.

Abstract

The Chromosome-centric Human Proteome Project (C-HPP), announced in September 2016, is an initiative to accelerate progress on the detection and characterization of neXtProt PE2,3,4 "missing proteins" (MPs) with a mandate to each chromosome team to find about 50 MPs over 2 years. Here we report major progress toward the neXt-MP50 challenge with 43 newly validated Chr 17 PE1 proteins, of which 25 were based on mass spectrometry, 12 on protein-protein interactions, 3 on a combination of MS and PPI, and 3 with other types of data. Notable among these new PE1 proteins were five keratin-associated proteins, a single olfactory receptor, and five additional membrane-embedded proteins. We evaluate the prospects of finding the remaining 105 MPs coded for on Chr 17, focusing on mass spectrometry and protein-protein interaction approaches. We present a list of 35 prioritized MPs with specific approaches that may be used in further MS and PPI experimental studies. Additionally, we demonstrate how in silico studies can be used to capture individual peptides from major data repositories, documenting one MP that appears to be a strong candidate for PE1. We are close to our goal of finding 50 MPs for Chr 17.

摘要

染色体中心的人类蛋白质组计划(C-HPP)于 2016 年 9 月宣布,旨在加速检测和描述下一个蛋白(neXtProt PE2,3,4)的进展,该计划要求每个染色体团队在两年内找到约 50 个 MPs。在这里,我们报告了在 neXt-MP50 挑战方面的重大进展,其中包括 43 个新验证的 Chr17PE1 蛋白,其中 25 个基于质谱,12 个基于蛋白质-蛋白质相互作用,3 个基于 MS 和 PPI 的组合,还有 3 个基于其他类型的数据。在这些新的 PE1 蛋白中,有 5 个角蛋白相关蛋白、1 个嗅觉受体和 5 个额外的膜嵌入蛋白。我们评估了在 Chr17 上找到其余 105 个编码 MPs 的前景,重点关注质谱和蛋白质-蛋白质相互作用方法。我们提出了一个有 35 个优先考虑的 MPs 的列表,并提供了可能用于进一步 MS 和 PPI 实验研究的具体方法。此外,我们展示了如何使用计算研究从主要数据存储库中捕获单个肽,记录一个似乎是 PE1 的强有力候选者的 MP。我们已经接近在 Chr17 上找到 50 个 MPs 的目标。

相似文献

2
The 2023 Report on the Proteome from the HUPO Human Proteome Project.2023 年人类蛋白质组组织蛋白质组报告。
J Proteome Res. 2024 Feb 2;23(2):532-549. doi: 10.1021/acs.jproteome.3c00591. Epub 2024 Jan 17.
7
The 2022 Report on the Human Proteome from the HUPO Human Proteome Project.《人类蛋白质组组织 2022 年人类蛋白质组报告》。
J Proteome Res. 2023 Apr 7;22(4):1024-1042. doi: 10.1021/acs.jproteome.2c00498. Epub 2022 Nov 1.
9
Advances in the Chromosome-Centric Human Proteome Project: looking to the future.染色体为中心的人类蛋白质组计划的进展:展望未来。
Expert Rev Proteomics. 2017 Dec;14(12):1059-1071. doi: 10.1080/14789450.2017.1394189. Epub 2017 Nov 10.

引用本文的文献

本文引用的文献

2
The target landscape of clinical kinase drugs.临床激酶药物的目标格局。
Science. 2017 Dec 1;358(6367). doi: 10.1126/science.aan4368.
10
The BioGRID interaction database: 2017 update.生物通用互作数据库:2017年更新版。
Nucleic Acids Res. 2017 Jan 4;45(D1):D369-D379. doi: 10.1093/nar/gkw1102. Epub 2016 Dec 14.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验