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人类蛋白质组组织(HUPO)脑蛋白质组计划试点研究中在人类大脑中鉴定出的蛋白质的功能注释。

Functional annotation of proteins identified in human brain during the HUPO Brain Proteome Project pilot study.

作者信息

Mueller Michael, Martens Lennart, Reidegeld Kai A, Hamacher Michael, Stephan Christian, Blüggel Martin, Körting Gerhard, Chamrad Daniel, Scheer Christian, Marcus Katrin, Meyer Helmut E, Apweiler Rolf

机构信息

EMBL Outstation, European Bioinformatics Institute, Wellcome Trust Genome Campus, Cambridge, UK.

出版信息

Proteomics. 2006 Sep;6(18):5059-75. doi: 10.1002/pmic.200600194.

Abstract

The HUPO Brain Proteome Project is an initiative coordinating proteomics studies to characterise human and mouse brain proteomes. Proteins identified in human brain samples during the project's pilot phase were put into biological context through integration with various annotation sources followed by a bioinformatics analysis. The data set was related to the genome sequence via the genes encoding identified proteins including an assessment of splice variant identification as well as an analysis of tissue specificity of the respective transcripts. Proteins were furthermore categorised according to subcellular localisation, molecular function and biological process, grouped into protein families and mapped to biological pathways they are known to act in. Involvement in pathological conditions was examined based on association with entries in the online version of Mendelian Inheritance in Man and an interaction network was derived from curated protein-proteininteraction data. Overall a non-redundant set of 1804 proteins was identified in human brain samples. In the majority of cases splice variants could be unambiguously identified by unique peptides, including matches to several hypothetical transcripts of known as well as predicted genes.

摘要

人类蛋白质组组织脑蛋白质组计划是一项协调蛋白质组学研究以表征人类和小鼠脑蛋白质组的倡议。在该计划的试点阶段,通过与各种注释来源整合并进行生物信息学分析,将在人类脑样本中鉴定出的蛋白质置于生物学背景中。通过编码已鉴定蛋白质的基因,该数据集与基因组序列相关,包括剪接变体鉴定评估以及各自转录本的组织特异性分析。此外,蛋白质根据亚细胞定位、分子功能和生物学过程进行分类,分组为蛋白质家族,并映射到它们已知作用的生物途径。基于与《人类孟德尔遗传》在线版本条目的关联,研究了其在病理状况中的参与情况,并从经过整理的蛋白质-蛋白质相互作用数据中得出了一个相互作用网络。总体而言,在人类脑样本中鉴定出了一组1804种非冗余蛋白质。在大多数情况下,剪接变体可以通过独特的肽段明确鉴定,包括与已知以及预测基因的几种假设转录本的匹配。

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