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莱茵衣藻绿藻中的亚蛋白质组分析。

Sub-proteome analysis in the green flagellate alga Chlamydomonas reinhardtii.

作者信息

Wagner Volker, Boesger Jens, Mittag Maria

机构信息

Institute of General Botany and Plant Physiology, Friedrich-Schiller-University Jena, 07743 Jena, Germany.

出版信息

J Basic Microbiol. 2009 Feb;49(1):32-41. doi: 10.1002/jobm.200800292.

Abstract

In the past years, research on the flagellate unicellular alga Chlamydomonas reinhardtii has entered a new era based on the availability of its complete genome. Since this green alga can be grown relatively easy in a short time-range, sufficient biological material is available to efficiently establish biochemical purification procedures of sub-cellular fractions. Combined with the available genome sequences, this paved the way to perform analysis of specific sub-proteomes by mass spectrometry. In this review, several approaches that provided comprehensive lists of components of certain sub-cellular compartments and their biological relevance will be described. These include proteins of chloroplast ribosomes, of flagella, of the eyespot as well as posttranslational and environmentally modified sub-proteomes. The power of such proteome approaches lies in the identification of novel components and modifications of a given sub-proteome that have not been discovered before. Information is usually gained at a large scale and is very valuable to further understand biological processes of a given cellular sub-compartment. But clearly the arduous task has then to be performed to further analyze the function of specific proteins/genes by RNA interference technology, mutant analyses or methods for identifying the protein interaction network within a sub-proteome.

摘要

在过去几年中,基于莱茵衣藻完整基因组的可得性,对这种鞭毛单细胞藻类的研究进入了一个新时代。由于这种绿藻能够在较短时间内相对容易地培养,因此有足够的生物材料来有效地建立亚细胞组分的生化纯化程序。结合现有的基因组序列,这为通过质谱分析特定亚蛋白质组铺平了道路。在这篇综述中,将描述几种能够提供某些亚细胞区室成分及其生物学相关性的综合列表的方法。这些包括叶绿体核糖体、鞭毛、眼点的蛋白质,以及翻译后修饰和环境修饰的亚蛋白质组。这种蛋白质组学方法的优势在于能够鉴定给定亚蛋白质组中以前未被发现的新成分和修饰。通常可以大规模获取信息,这对于进一步理解给定细胞亚区室的生物学过程非常有价值。但显然,接下来还需要通过RNA干扰技术、突变分析或识别亚蛋白质组内蛋白质相互作用网络的方法来进一步分析特定蛋白质/基因的功能,这是一项艰巨的任务。

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