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本文引用的文献

1
False discovery rates of protein identifications: a strike against the two-peptide rule.蛋白质鉴定的错误发现率:对双肽规则的一次打击。
J Proteome Res. 2009 Sep;8(9):4173-81. doi: 10.1021/pr9004794.
2
EPIC-DB: a proteomics database for studying Apicomplexan organisms.EPIC-DB:一个用于研究顶复门生物的蛋白质组学数据库。
BMC Genomics. 2009 Jan 21;10:38. doi: 10.1186/1471-2164-10-38.
3
Computational analysis and experimental validation of gene predictions in Toxoplasma gondii.刚地弓形虫基因预测的计算分析与实验验证
PLoS One. 2008;3(12):e3899. doi: 10.1371/journal.pone.0003899. Epub 2008 Dec 9.
4
PredGPI: a GPI-anchor predictor.PredGPI:一种糖基磷脂酰肌醇锚定预测器。
BMC Bioinformatics. 2008 Sep 23;9:392. doi: 10.1186/1471-2105-9-392.
5
Three-layer sandwich gel electrophoresis: a method of salt removal and protein concentration in proteome analysis.三层夹心凝胶电泳:蛋白质组分析中的一种盐去除和蛋白质浓缩方法。
J Proteome Res. 2008 Oct;7(10):4256-65. doi: 10.1021/pr800182b. Epub 2008 Sep 17.
6
Population structure of Toxoplasma gondii: clonal expansion driven by infrequent recombination and selective sweeps.刚地弓形虫的种群结构:由罕见重组和选择性清除驱动的克隆性扩张
Annu Rev Microbiol. 2008;62:329-51. doi: 10.1146/annurev.micro.62.081307.162925.
7
Assigning significance to peptides identified by tandem mass spectrometry using decoy databases.使用诱饵数据库对通过串联质谱鉴定的肽段赋予显著性。
J Proteome Res. 2008 Jan;7(1):29-34. doi: 10.1021/pr700600n. Epub 2007 Dec 8.
8
Kiss and spit: the dual roles of Toxoplasma rhoptries.亲吻与吐出:弓形虫棒状体的双重作用
Nat Rev Microbiol. 2008 Jan;6(1):79-88. doi: 10.1038/nrmicro1800.
9
Congenital and acquired toxoplasmosis: diversity and role of antibodies in different compartments of the host.先天性和获得性弓形虫病:抗体在宿主不同部位的多样性及作用
Parasite Immunol. 2007 Dec;29(12):651-60. doi: 10.1111/j.1365-3024.2007.00982.x.
10
Proteomics of integral membrane proteins--theory and application.整合膜蛋白的蛋白质组学——理论与应用
Chem Rev. 2007 Aug;107(8):3687-714. doi: 10.1021/cr068286z.

弓形虫膜蛋白的综合蛋白质组学分析。

Comprehensive proteomic analysis of membrane proteins in Toxoplasma gondii.

机构信息

Department of Pathology, Biodefense Proteomics Research Center, Albert Einstein College of Medicine, Bronx, NY 10461, USA.

出版信息

Mol Cell Proteomics. 2011 Jan;10(1):M110.000745. doi: 10.1074/mcp.M110.000745. Epub 2010 Oct 10.

DOI:10.1074/mcp.M110.000745
PMID:20935347
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3013445/
Abstract

Toxoplasma gondii (T. gondii) is an obligate intracellular protozoan parasite that is an important human and animal pathogen. Experimental information on T. gondii membrane proteins is limited, and the majority of gene predictions with predicted transmembrane motifs are of unknown function. A systematic analysis of the membrane proteome of T. gondii is important not only for understanding this parasite's invasion mechanism(s), but also for the discovery of potential drug targets and new preventative and therapeutic strategies. Here we report a comprehensive analysis of the membrane proteome of T. gondii, employing three proteomics strategies: one-dimensional gel liquid chromatography-tandem MS analysis (one-dimensional gel electrophoresis LC-MS/MS), biotin labeling in conjunction with one-dimensional gel LC-MS/MS analysis, and a novel strategy that combines three-layer "sandwich" gel electrophoresis with multidimensional protein identification technology. A total of 2241 T. gondii proteins with at least one predicted transmembrane segment were identified and grouped into 841 sequentially nonredundant protein clusters, which account for 21.8% of the predicted transmembrane protein clusters in the T. gondii genome. A large portion (42%) of the identified T. gondii membrane proteins are hypothetical proteins. Furthermore, many of the membrane proteins validated by mass spectrometry are unique to T. gondii or to the Apicomplexa, providing a set of gene predictions ripe for experimental investigation, and potentially suitable targets for the development of therapeutic strategies.

摘要

刚地弓形虫(Toxoplasma gondii)是一种专性细胞内原生动物寄生虫,是重要的人类和动物病原体。关于刚地弓形虫膜蛋白的实验信息有限,并且具有预测跨膜基序的大多数基因预测的功能未知。刚地弓形虫膜蛋白质组的系统分析不仅对于理解这种寄生虫的入侵机制很重要,而且对于发现潜在的药物靶点和新的预防和治疗策略也很重要。在这里,我们报告了刚地弓形虫膜蛋白质组的全面分析,采用了三种蛋白质组学策略:一维凝胶液相色谱 - 串联 MS 分析(一维凝胶电泳 LC-MS/MS),生物素标记结合一维凝胶 LC-MS/MS 分析,以及一种将三层“三明治”凝胶电泳与多维蛋白质鉴定技术相结合的新策略。总共鉴定了 2241 种具有至少一个预测跨膜片段的刚地弓形虫蛋白,并将其分为 841 个顺序非冗余蛋白簇,占刚地弓形虫基因组中预测跨膜蛋白簇的 21.8%。鉴定的刚地弓形虫膜蛋白的很大一部分(42%)是假设蛋白。此外,许多通过质谱验证的膜蛋白是刚地弓形虫或顶复门特有的,为实验研究提供了一组成熟的基因预测,并且可能适合开发治疗策略的靶点。