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通过靶向蛋白质组学对拟南芥质膜转运组进行分析。

Towards the profiling of the Arabidopsis thaliana plasma membrane transportome by targeted proteomics.

机构信息

Laboratoire de Protéomique Fonctionnelle, INRA UR1199, Montpellier, France.

出版信息

Proteomics. 2011 May;11(9):1789-97. doi: 10.1002/pmic.201000660. Epub 2011 Mar 17.

DOI:10.1002/pmic.201000660
PMID:21413151
Abstract

Plant membranes bear a variety of transporters belonging to multigene families that are affected by environmental and nutritional conditions. In addition, they often display high-sequence identity, making difficult in-depth investigation by current shot-gun strategies. In this study, we set up a targeted proteomics approach aimed at identifying and quantifying within single experiments the five major proton pumps of the autoinhibited H(+) ATPases (AHA) family, the 13 plasma membrane intrinsic proteins (PIP) water channels (PIPs), and ten members of ammonium transporters (AMTs) and nitrate transporter (NRT) families. Proteotypic peptides were selected and isotopically labeled heavy versions were used for technical optimization and for quantification of the corresponding light version in biological samples. This approach allowed to quantify simultaneously nine PIPs in leaf membranes and 13 PIPs together with three autoinhibited H(+) ATPases, two ammonium transporters, and two NRTs in root membranes. Similarly, it was used to investigate the effect of a salt stress on the expression of these latter 20 transporters in roots. These novel isoform-specific data were compared with published transcriptome information and revealed a close correlation between PIP isoforms and transcripts levels. The obtained resource is reusable and can be expanded to other transporter families for large-scale profiling of membrane transporters.

摘要

植物膜上带有多种属于多基因家族的转运蛋白,这些转运蛋白会受到环境和营养条件的影响。此外,它们通常具有高度的序列同一性,这使得当前的高通量策略难以进行深入研究。在这项研究中,我们建立了一种靶向蛋白质组学方法,旨在在单个实验中鉴定和定量 5 种自动抑制 H(+)ATP 酶(AHA)家族的主要质子泵、13 种质膜内在蛋白(PIP)水通道(PIPs)以及 10 种铵转运体(AMTs)和硝酸盐转运体(NRT)家族成员。选择了代表性肽段,并使用同位素标记的重版本进行技术优化,并对生物样品中的相应轻版本进行定量。该方法可同时定量叶膜中的 9 种 PIP 和根膜中的 13 种 PIP 以及 3 种自动抑制 H(+)ATP 酶、2 种铵转运体和 2 种 NRT。同样,它被用于研究盐胁迫对这些后 20 种转运体在根部表达的影响。这些新的同工型特异性数据与已发表的转录组信息进行了比较,揭示了 PIP 同工型与转录物水平之间的密切相关性。所获得的资源是可重复使用的,可以扩展到其他转运体家族,以大规模分析膜转运体。

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