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通过代谢标记和质谱法测定拟南芥叶片和根组织中完整质膜蛋白的相对丰度。

Relative abundance of integral plasma membrane proteins in Arabidopsis leaf and root tissue determined by metabolic labeling and mass spectrometry.

机构信息

Department of Biochemistry and Structural Biology, Center for Molecular Protein Science, Lund University, Lund, Sweden.

出版信息

PLoS One. 2013 Aug 19;8(8):e71206. doi: 10.1371/journal.pone.0071206. eCollection 2013.

DOI:10.1371/journal.pone.0071206
PMID:23990937
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3747180/
Abstract

Metabolic labeling of proteins with a stable isotope ((15)N) in intact Arabidopsis plants was used for accurate determination by mass spectrometry of differences in protein abundance between plasma membranes isolated from leaves and roots. In total, 703 proteins were identified, of which 188 were predicted to be integral membrane proteins. Major classes were transporters, receptors, proteins involved in membrane trafficking and cell wall-related proteins. Forty-one of the integral proteins, including nine of the 13 isoforms of the PIP (plasma membrane intrinsic protein) aquaporin subfamily, could be identified by peptides unique to these proteins, which made it possible to determine their relative abundance in leaf and root tissue. In addition, peptides shared between isoforms gave information on the proportions of these isoforms. A comparison between our data for protein levels and corresponding data for mRNA levels in the widely used database Genevestigator showed an agreement for only about two thirds of the proteins. By contrast, localization data available in the literature for 21 of the 41 proteins show a much better agreement with our data, in particular data based on immunostaining of proteins and GUS-staining of promoter activity. Thus, although mRNA levels may provide a useful approximation for protein levels, detection and quantification of isoform-specific peptides by proteomics should generate the most reliable data for the proteome.

摘要

在完整的拟南芥植物中用稳定同位素 ((15)N) 对蛋白质进行代谢标记,用于通过质谱法准确测定从叶片和根部分离的质膜之间蛋白质丰度的差异。总共鉴定出 703 种蛋白质,其中 188 种被预测为完整膜蛋白。主要类别是转运蛋白、受体、参与膜运输的蛋白质和与细胞壁相关的蛋白质。41 种完整蛋白质,包括 PIP(质膜内在蛋白)水通道蛋白亚家族的 13 个同工型中的 9 个,可以通过这些蛋白质特有的肽来识别,这使得可以确定它们在叶和根组织中的相对丰度。此外,同工型之间共享的肽提供了这些同工型的比例信息。我们对蛋白质水平的数据与广泛使用的 Genevestigator 数据库中相应的 mRNA 水平数据进行比较,发现只有大约三分之二的蛋白质是一致的。相比之下,文献中可用于 41 种蛋白质中的 21 种蛋白质的定位数据与我们的数据更吻合,特别是基于蛋白质免疫染色和启动子活性的 GUS 染色的数据。因此,尽管 mRNA 水平可能为蛋白质水平提供有用的近似值,但通过蛋白质组学检测和定量同工型特异性肽应该为蛋白质组生成最可靠的数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92a0/3747180/d766abdae907/pone.0071206.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92a0/3747180/fe1b752ded3d/pone.0071206.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92a0/3747180/d2f6d5e67707/pone.0071206.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92a0/3747180/bb83de738e1c/pone.0071206.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92a0/3747180/74a32a39eefa/pone.0071206.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92a0/3747180/e91c1273ecce/pone.0071206.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92a0/3747180/3efc055056b1/pone.0071206.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92a0/3747180/d766abdae907/pone.0071206.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92a0/3747180/fe1b752ded3d/pone.0071206.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92a0/3747180/d2f6d5e67707/pone.0071206.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92a0/3747180/bb83de738e1c/pone.0071206.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92a0/3747180/74a32a39eefa/pone.0071206.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92a0/3747180/e91c1273ecce/pone.0071206.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92a0/3747180/3efc055056b1/pone.0071206.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92a0/3747180/d766abdae907/pone.0071206.g007.jpg

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