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PLoS One. 2011 Feb 23;6(2):e17287. doi: 10.1371/journal.pone.0017287.
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Discussion on common data analysis strategies used in MS-based proteomics.基于 MS 的蛋白质组学中常用数据分析策略的探讨。
Proteomics. 2011 Feb;11(4):604-19. doi: 10.1002/pmic.201000404. Epub 2011 Jan 17.
3
SurreyFBA: a command line tool and graphics user interface for constraint-based modeling of genome-scale metabolic reaction networks.SurreyFBA:一种用于基于约束的基因组规模代谢反应网络建模的命令行工具和图形用户界面。
Bioinformatics. 2011 Feb 1;27(3):433-4. doi: 10.1093/bioinformatics/btq679. Epub 2010 Dec 9.
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Revealing the molecular relationship between type 2 diabetes and the metabolic changes induced by a very-low-carbohydrate low-fat ketogenic diet.揭示 2 型糖尿病与极低碳水化合物、低脂肪生酮饮食所引起的代谢变化之间的分子关系。
Nutr Metab (Lond). 2010 Dec 9;7:88. doi: 10.1186/1743-7075-7-88.
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Analysis of the urine proteome in patients with pancreatic ductal adenocarcinoma.胰腺导管腺癌患者尿液蛋白质组分析。
Proteomics Clin Appl. 2008 Jul;2(7-8):1047-57. doi: 10.1002/prca.200780164. Epub 2008 Jul 10.
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Patterns of human gene expression variance show strong associations with signaling network hierarchy.人类基因表达变异模式与信号网络层次结构显示出强烈关联。
BMC Syst Biol. 2010 Nov 12;4:154. doi: 10.1186/1752-0509-4-154.
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Gene regulatory network reveals oxidative stress as the underlying molecular mechanism of type 2 diabetes and hypertension.基因调控网络揭示氧化应激是 2 型糖尿病和高血压的潜在分子机制。
BMC Med Genomics. 2010 Oct 13;3:45. doi: 10.1186/1755-8794-3-45.
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Urinary collagen fragments are significantly altered in diabetes: a link to pathophysiology.在糖尿病中,尿胶原蛋白片段发生显著改变:与病理生理学相关联。
PLoS One. 2010 Sep 28;5(9):e13051. doi: 10.1371/journal.pone.0013051.
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High-efficiency nano- and micro-HPLC--high-resolution Orbitrap-MS platform for top-down proteomics.高效纳微液相色谱-高分辨轨道阱质谱平台用于从头蛋白质组学研究。
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10
Top-down protein characterization facilitated by ion/ion reactions on a quadrupole/time of flight platform.基于四极杆/飞行时间平台的离子/离子反应实现的自上而下的蛋白质特征分析。
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蛋白质组学与系统生物学:营养科学中的当前与未来应用。

Proteomics and systems biology: current and future applications in the nutritional sciences.

机构信息

Nutritional Sciences Division, University of Surrey, Guildford, Surrey, UK.

出版信息

Adv Nutr. 2011 Jul;2(4):355-64. doi: 10.3945/an.111.000554. Epub 2011 Jun 28.

DOI:10.3945/an.111.000554
PMID:22332076
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3125684/
Abstract

In the last decade, advances in genomics, proteomics, and metabolomics have yielded large-scale datasets that have driven an interest in global analyses, with the objective of understanding biological systems as a whole. Systems biology integrates computational modeling and experimental biology to predict and characterize the dynamic properties of biological systems, which are viewed as complex signaling networks. Whereas the systems analysis of disease-perturbed networks holds promise for identification of drug targets for therapy, equally the identified critical network nodes may be targeted through nutritional intervention in either a preventative or therapeutic fashion. As such, in the context of the nutritional sciences, it is envisioned that systems analysis of normal and nutrient-perturbed signaling networks in combination with knowledge of underlying genetic polymorphisms will lead to a future in which the health of individuals will be improved through predictive and preventative nutrition. Although high-throughput transcriptomic microarray data were initially most readily available and amenable to systems analysis, recent technological and methodological advances in MS have contributed to a linear increase in proteomic investigations. It is now commonplace for combined proteomic technologies to generate complex, multi-faceted datasets, and these will be the keystone of future systems biology research. This review will define systems biology, outline current proteomic methodologies, highlight successful applications of proteomics in nutrition research, and discuss the challenges for future applications of systems biology approaches in the nutritional sciences.

摘要

在过去的十年中,基因组学、蛋白质组学和代谢组学的进展产生了大规模数据集,这激发了人们对全局分析的兴趣,旨在全面了解生物系统。系统生物学将计算建模和实验生物学相结合,以预测和描述生物系统的动态特性,这些系统被视为复杂的信号网络。虽然对疾病干扰网络的系统分析有望为治疗药物靶点的确定提供帮助,但同样可以通过营养干预以预防或治疗的方式针对已识别的关键网络节点。因此,在营养科学领域,可以预见的是,对正常和营养干扰信号网络的系统分析与对潜在遗传多态性的了解相结合,将引领未来通过预测和预防营养来改善个体健康。尽管高通量转录组微阵列数据最初最容易获得且适合系统分析,但 MS 技术的最新技术和方法进展促进了蛋白质组学研究的线性增加。现在,结合蛋白质组学技术生成复杂、多方面数据集已经很常见,这些将成为未来系统生物学研究的基石。本文将定义系统生物学,概述当前的蛋白质组学方法,强调蛋白质组学在营养研究中的成功应用,并讨论系统生物学方法在营养科学中未来应用的挑战。