Wittek Oliver, Jahreis Bastian, Römpp Andreas
Bioanalytical Sciences and Food Analysis, University of Bayreuth, Universitaetsstrasse 30, D-95447 Bayreuth, Germany.
Anal Chem. 2023 Oct 10;95(40):14972-14980. doi: 10.1021/acs.analchem.3c02428. Epub 2023 Sep 25.
Matrix-assisted laser desorption/ionization mass spectrometry (MALDI MS) imaging following in situ enzymatic digestion is a versatile analytical method for the untargeted investigation of protein distributions, which has rarely been used for plants so far. The present study describes a workflow for in situ tryptic digestion of plant seed tissue for MALDI MS imaging. Substantial modifications to the sample preparation procedure for mammalian tissues were necessary to cater to the specific properties of plant materials. For the first time, distributions of tryptic peptides were successfully visualized in plant tissue using MS imaging with accurate mass detection. Sixteen proteins were visualized and identified in chickpea seeds showing different distribution patterns, e.g., in the cotyledons, radicle, or testa. All tryptic peptides were detected with a mass resolution higher than 60,000 as well as a mass accuracy better than 1.5 ppm root-mean-square error and were matched to results from complementary liquid chromatography-MS/MS (LC-MS/MS) data. The developed method was also applied to crab's eye vine seeds for targeted MS imaging of the toxic protein abrin, showing the presence of abrin-a in all compartments. Abrin (59 kDa), as well as the majority of proteins visualized in chickpeas, was larger than 50 kDa and would thus not be readily accessible by top-down MS imaging. Since antibodies for plant proteins are often not readily available, in situ digestion MS imaging provides unique information, as it makes the distribution and identification of larger proteins in plant tissues accessible in an untargeted manner. This opens up new possibilities in the field of plant science as well as to assess the nutritional quality and/or safety of crops.
原位酶解后的基质辅助激光解吸/电离质谱(MALDI MS)成像,是一种用于非靶向研究蛋白质分布的通用分析方法,目前在植物研究中很少使用。本研究描述了一种用于植物种子组织原位胰蛋白酶消化以进行MALDI MS成像的工作流程。为了适应植物材料的特殊性质,对哺乳动物组织的样品制备程序进行了大量修改。首次使用具有精确质量检测的MS成像技术成功地在植物组织中可视化了胰蛋白酶肽的分布。在鹰嘴豆种子中可视化并鉴定了16种蛋白质,它们呈现出不同的分布模式,例如在子叶、胚根或种皮中。所有胰蛋白酶肽的质量分辨率均高于60,000,质量准确度优于1.5 ppm均方根误差,并与互补液相色谱 - 质谱/质谱(LC-MS/MS)数据的结果相匹配。所开发的方法还应用于鸡骨草种子,用于对有毒蛋白相思子毒素进行靶向MS成像,结果表明在所有部分均存在相思子毒素-a。相思子毒素(59 kDa)以及在鹰嘴豆中可视化的大多数蛋白质都大于50 kDa,因此自上而下的MS成像难以直接检测到。由于植物蛋白的抗体通常不易获得,原位消化MS成像提供了独特的信息,因为它能够以非靶向方式获取植物组织中较大蛋白质的分布和鉴定信息。这为植物科学领域以及评估作物的营养质量和/或安全性开辟了新的可能性。