首页> 外文期刊>Rapid Communications in Mass Spectrometry: RCM >Structural studies of glutenin subunits 1Dy10 and 1Dy12 by matrix-assisted laser desorption/ionisation mass spectrometry and high-performance liquid chromatography/electrospray ionisation mass spectrometry
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Structural studies of glutenin subunits 1Dy10 and 1Dy12 by matrix-assisted laser desorption/ionisation mass spectrometry and high-performance liquid chromatography/electrospray ionisation mass spectrometry

机译:通过基质辅助激光解吸/电离质谱和高效液相色谱/电喷雾电离质谱研究谷蛋白亚基1Dy10和1Dy12的结构

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Structural studies of the high molecular weight (HMW) glutenin subunits 1Dy10 and 1Dy12 of bread wheat were conducted using matrix-assisted laser desorption/ionisation time-of-flight mass spectrometry (MALDI-TOFMS) and reversed-phase high-performance liquid chromatography/electrospray ionisation mass spectrometry (RP-HPLC/ESI-MS). For both proteins, MALDI-TOFMS analysis showed that the isolated fractions contained a second component with a mass about 500-540 Da lower than the major component. The testing and correction of the gene-derived amino acid sequences of both proteins were performed by direct MALDI-TOFMS analysis of their tryptic peptide mixture and analysis of the digests was performed by recording several MALDI mass spectra of the mixture at low, medium and high mass ranges, optimising the matrix and the acquisition parameters for each mass range. Complementary data were obtained by RP-HPLC/ESI-MS analysis of the tryptic digest. This resulted in the coverage of the whole protein sequences except for two short fragments (T1 and T8), which are identical in the two homologous subunits, and for an additional dipeptide (T14) in subunit 1Dy12, which were not detected. It also demonstrated that, in contrast to the gene-derived data, the sequence of subunit 1Dy12 does not include the dipeptide Gly-Gln between residues Gln(454) and Pro(455), and that the lower mass components present in both fractions correspond to the same sequences lacking short peptides that are probably lost from the protein N- or C-termini. Finally, the results obtained provide evidence for the, lack of a substantial level of glycosylation or other post-translational modifications of the two subunits, and demonstrate that mass spectrometric mapping is the most useful method presently available for tile direct verification of the gene-derived sequences of HMW glutenin subunits and similar proteins. Copyright (C) 2003 John Wiley Sons, Ltd. [References: 21]
机译:使用基质辅助激光解吸/电离飞行时间质谱(MALDI-TOFMS)和反相高效液相色谱/电喷雾电离质谱(RP-HPLC / ESI-MS)。对于这两种蛋白质,MALDI-TOFMS分析表明,分离出的级分包含质量比主要组分低约500-540 Da的第二组分。通过直接对其胰蛋白酶肽混合物进行MALDI-TOFMS分析,对两种蛋白质的基因衍生氨基酸序列进行测试和校正,并通过记录混合物在低,中和高温度下的几种MALDI质谱图来进行消化物分析。质量范围,针对每个质量范围优化矩阵和采集参数。补充数据通过胰蛋白酶消化物的RP-HPLC / ESI-MS分析获得。这导致整个蛋白质序列的覆盖,除了两个短片段(T1和T8)(在两个同源亚基中是相同的),以及未被检测到的亚肽1Dy12中的另一个二肽(T14)。还证明,与基因衍生数据相反,亚基1Dy12的序列在残基Gln(454)和Pro(455)之间不包含二肽Gly-Gln,并且两个馏分中存在的较低质量组分相对应缺失短肽的相同序列可能会从蛋白N端或C端丢失。最后,获得的结果为缺乏足够水平的两个亚基的糖基化或其他翻译后修饰提供了证据,并证明了质谱定位是目前可用于直接验证基因衍生的最有用的方法HMW谷蛋白亚基和类似蛋白质的序列。版权所有(C)2003 John Wiley Sons,Ltd. [引用:21]

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