López-Ferrer Daniel, Heibeck Tyler H, Petritis Konstantinos, Hixson Kim K, Qian Weijun, Monroe Matthew E, Mayampurath Anoop, Moore Ronald J, Belov Mikhail E, Camp David G, Smith Richard D
Biological Science Division and Environmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, Washington 99352, USA.
J Proteome Res. 2008 Sep;7(9):3860-7. doi: 10.1021/pr800161x. Epub 2008 Aug 8.
A new sample processing workflow that uses high intensity focused ultrasound to rapidly reduce and alkylate cysteines, digest proteins and then label peptides with (18)O was developed for quantitative proteomics applications. Each step was individually refined to minimize reaction times, peptide loses and undesired byproducts or modifications. When this novel workflow was used, mouse plasma proteins were successfully denatured, alkylated, in-solution digested, and (18)O-labeled in <10 min for subsequent analysis by liquid chromatography-electrospray ionization high resolution mass spectrometry. Performance was evaluated in terms of the number of mouse plasma peptides and proteins identified in a shotgun approach and the quantitative dynamic range. The results were compared with previously published results obtained using conventional sample preparation methods and were found to be similar. Advantages of the new method include greatly simplified and accelerated sample processing, as well as being readily amenable to automation.
为定量蛋白质组学应用开发了一种新的样品处理工作流程,该流程使用高强度聚焦超声快速还原和烷基化半胱氨酸、消化蛋白质,然后用¹⁸O标记肽段。对每个步骤进行了单独优化,以尽量减少反应时间、肽段损失以及不需要的副产物或修饰。使用这种新颖的工作流程时,小鼠血浆蛋白在不到10分钟的时间内成功变性、烷基化、溶液内消化并进行¹⁸O标记,随后通过液相色谱 - 电喷雾电离高分辨率质谱进行分析。根据鸟枪法鉴定出的小鼠血浆肽段和蛋白质数量以及定量动态范围对性能进行了评估。将结果与使用传统样品制备方法获得的先前发表的结果进行比较,发现结果相似。新方法的优点包括大大简化和加速了样品处理,并且易于实现自动化。