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Quantitative LC-MS proteoform profiling of intact wheat glutenin subunits

机译:完整小麦谷蛋白亚基的定量LC-MS蛋白质谱分析

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Methodology for the quantitative analysis of intact glutenin proteins by ESI-LC-MS was developed with 1 Da mass resolution, constituting the first published application of proteoform profiling to plant biology. Two parent lines and 28 F5 crosses were analyzed in two blocks, 14 months apart. Control sample data were used to align retention times and normalize abundance between sample sets. A total of 4622 observations of 347 distinct proteoforms between 17 899 and 88 744 Da were observed. Proteoform abundances spanned a 1000-fold range and were linear (r(2) > 0.990) with dilution. A novel method for the objective elimination of low intensity, noise-dominated data using replicate variability within the dataset is presented. Two abundant PTMs were detected; one known but uncharacterized Bx and Dy high-molecular-weight glutenin subunit (HMWGS) PTM and the other in 24 low molecular weight proteoform pairs. Finally, 16 abundant proteoforms were detected in progeny but not in either parent. This application should increase the statistical power of correlations between gluten complement and functional data and drive the detection of novel PTMs that may indicate differential regulation of the cellular processes related to quality.
机译:通过ESI-LC-MS对完整谷蛋白蛋白的定量分析的方法,具有1A大规模分辨率,构成第一次公布的植物生物学植物生物学的公开应用。分别为14个月,分析了两个母线和28个F5横斜体。控制样品数据用于对准保留时间并使样品集之间的丰富度正常化。在17899和88 744Da之间观察到347个不同的蛋白质常规的4622个观察结果。蛋白质Oform丰度截止了1000倍的范围,并具有稀释的线性(R(2)> 0.990)。提出了一种用于客观消除低强度,使用数据集中的复制可变性的低强度的噪声主导数据的新方法。检测到两个丰富的PTM;一种已知但无特异化的Bx和Dy高分子重量谷蛋白亚基(HMWGs)Ptm,另一个在24个低分子量蛋白质成对中。最后,在后代检测到16种丰富的蛋白质ort,但不在任何一种父母中。该应用应该增加面筋补充剂和功能数据之间的相关性的统计功率,并驱动了可能表示与质量相关的细胞过程的差异调节的新型PTM的检测。

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