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植物稳定同位素标记氨基酸法:用于拟南芥幼苗定量蛋白质组学的氨基酸稳定同位素标记

Plant SILAC: stable-isotope labelling with amino acids of arabidopsis seedlings for quantitative proteomics.

作者信息

Lewandowska Dominika, ten Have Sara, Hodge Kelly, Tillemans Vinciane, Lamond Angus I, Brown John W S

机构信息

Cell and Molecular Sciences, The James Hutton Institute, Dundee, United Kingdom.

出版信息

PLoS One. 2013 Aug 20;8(8):e72207. doi: 10.1371/journal.pone.0072207. eCollection 2013.

Abstract

Stable Isotope Labelling by Amino acids in Cell culture (SILAC) is a powerful technique for comparative quantitative proteomics, which has recently been applied to a number of different eukaryotic organisms. Inefficient incorporation of labelled amino acids in cell cultures of Arabidopsis thaliana has led to very limited use of SILAC in plant systems. We present a method allowing, for the first time, efficient labelling with stable isotope-containing arginine and lysine of whole Arabidopsis seedlings. To illustrate the utility of this method, we have combined the high labelling efficiency (>95%) with quantitative proteomics analyses of seedlings exposed to increased salt concentration. In plants treated for 7 days with 80 mM NaCl, a relatively mild salt stress, 215 proteins were identified whose expression levels changed significantly compared to untreated seedling controls. The 92 up-regulated proteins included proteins involved in abiotic stress responses and photosynthesis, while the 123 down-regulated proteins were enriched in proteins involved in reduction of oxidative stress and other stress responses, respectively. Efficient labelling of whole Arabidopsis seedlings by this modified SILAC method opens new opportunities to exploit the genetic resources of Arabidopsis and analyse the impact of mutations on quantitative protein dynamics in vivo.

摘要

细胞培养中氨基酸稳定同位素标记法(SILAC)是一种用于比较定量蛋白质组学的强大技术,最近已应用于多种不同的真核生物。在拟南芥细胞培养中标记氨基酸的掺入效率低下,导致SILAC在植物系统中的应用非常有限。我们首次提出了一种方法,能够用含稳定同位素的精氨酸和赖氨酸对整个拟南芥幼苗进行高效标记。为了说明该方法的实用性,我们将高标记效率(>95%)与对暴露于增加盐浓度下的幼苗进行的定量蛋白质组学分析相结合。在用80 mM NaCl处理7天的植物中,这是一种相对温和的盐胁迫,鉴定出215种蛋白质,其表达水平与未处理的幼苗对照相比有显著变化。92种上调的蛋白质包括参与非生物胁迫反应和光合作用的蛋白质,而123种下调的蛋白质分别富含参与减轻氧化应激和其他胁迫反应的蛋白质。通过这种改良的SILAC方法对整个拟南芥幼苗进行高效标记,为利用拟南芥的遗传资源以及分析突变对体内定量蛋白质动态的影响开辟了新的机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/018e/3748079/7f180542732f/pone.0072207.g001.jpg

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