亲爱的研友该休息了!由于当前在线用户较少,发布求助请尽量完整地填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!身体可是革命的本钱,早点休息,好梦!

Quantitative Proteome and Transcriptome Analysis of the Archaeon Thermoplasma acidophilum Cultured under Aerobic and Anaerobic Conditions

蛋白质组 生物 转录组 蛋白质组学 定量蛋白质组学 嗜酸热浆菌 生物化学 基因 基因表达 计算生物学
作者
Na Sun,Cuiping Pan,Stephan Nickell,Matthias Mann,Wolfgang Baumeister,István Nagy
出处
期刊:Journal of Proteome Research [American Chemical Society]
卷期号:9 (9): 4839-4850 被引量:44
标识
DOI:10.1021/pr100567u
摘要

A comparative proteome and transcriptome analysis of Thermoplasma acidophilum cultured under aerobic and anaerobic conditions has been performed. One-thousand twenty-five proteins were identified covering 88% of the cytosolic proteome. Using a label-free quantitation method, we found that approximately one-quarter of the identified proteome (263 proteins) were significantly induced (>2 fold) under anaerobic conditions. Thirty-nine macromolecular complexes were identified, of which 28 were quantified and 15 were regulated under anaerobiosis. In parallel, a whole genome cDNA microarray analysis was performed showing that the expression levels of 445 genes were influenced by the absence of oxygen. Interestingly, more than 40% of the membrane protein-encoding genes (145 out of 335 ORFs) were up- or down-regulated at the mRNA level. Many of these proteins are functionally associated with extracellular protein or peptide degradation or ion and amino acid transport. Comparison of the transcriptome and proteome showed only a weak positive correlation between mRNA and protein expression changes, which is indicative of extensive post-transcriptional regulatory mechanisms in T. acidophilum. Integration of transcriptomics and proteomics data generated hypotheses for physiological adaptations of the cells to anaerobiosis, and the quantitative proteomics data together with quantitative analysis of protein complexes provide a platform for correlation of MS-based proteomics studies with cryo-electron tomography-based visual proteomics approaches.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
无极微光应助颜小超采纳,获得20
12秒前
负责的如萱完成签到,获得积分10
20秒前
OK应助科研通管家采纳,获得30
33秒前
Kao应助科研通管家采纳,获得10
33秒前
Kao应助科研通管家采纳,获得10
33秒前
daisy完成签到,获得积分10
33秒前
郗妫完成签到,获得积分10
35秒前
1分钟前
小泉完成签到 ,获得积分10
1分钟前
QCL发布了新的文献求助10
1分钟前
1分钟前
1分钟前
QCL完成签到,获得积分20
1分钟前
深情的朝雪完成签到,获得积分10
1分钟前
土土桔子糖完成签到 ,获得积分10
1分钟前
传奇3应助xyy采纳,获得10
1分钟前
平淡夏青完成签到,获得积分10
2分钟前
颜小超完成签到,获得积分10
2分钟前
深情安青应助CTS采纳,获得10
2分钟前
2分钟前
Kao应助科研通管家采纳,获得10
2分钟前
Kao应助科研通管家采纳,获得10
2分钟前
共享精神应助科研通管家采纳,获得10
2分钟前
Kao应助科研通管家采纳,获得10
2分钟前
颜小超发布了新的文献求助20
2分钟前
2分钟前
aa完成签到,获得积分10
2分钟前
CTS发布了新的文献求助10
2分钟前
无极微光应助颜小超采纳,获得20
2分钟前
李爱国应助yangwei采纳,获得30
3分钟前
默默的以柳完成签到,获得积分10
3分钟前
薤白完成签到 ,获得积分10
3分钟前
寒暑易节完成签到,获得积分20
3分钟前
苗条的傲安完成签到,获得积分10
3分钟前
Kao应助科研通管家采纳,获得10
4分钟前
陶醉之柔完成签到,获得积分10
4分钟前
大气青枫完成签到,获得积分10
5分钟前
Licy完成签到,获得积分10
5分钟前
share完成签到 ,获得积分10
5分钟前
xyy完成签到,获得积分20
5分钟前
高分求助中
Principles of Economics, 11th Edition 10000
University Physics with Modern Physics, 16th edition 10000
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Development of a Bridge Weigh-In-Motion System: A technology to convert the bridge response to the passage of traffic into data on vehicle configurations, speeds, times of travel and weights 1000
ズームレンズの光学設計に関する研究 800
Fundamentals of Pharmaceutical and Biologics Regulations: A Global Perspective, Second Edition 700
Matrix Methods in Data Mining and Pattern Recognition Second Edition 610
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7281842
求助须知:如何正确求助?哪些是违规求助? 8902737
关于积分的说明 18833465
捐赠科研通 6953122
什么是DOI,文献DOI怎么找? 3207531
关于科研通互助平台的介绍 2377815
邀请新用户注册赠送积分活动 2182700