Center for Integrated Protein Science at the Department of Chemistry, Ludwig-Maximilians-Universität München, Butenandtstr. 5-13, 81377, Munich, Germany.
Department of Molecular Biology &, the Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ, 08544, USA.
Angew Chem Int Ed Engl. 2018 Mar 5;57(11):2958-2962. doi: 10.1002/anie.201708867. Epub 2018 Feb 15.
Modern proteomics requires reagents for exact quantification of peptides in complex mixtures. Peptide labelling is most typically achieved with isobaric tags that consist of a balancer and a reporter part that separate in the gas phase. An ingenious distribution of stable isotopes provides multiple reagents with identical molecular weight but a different mass of the reporter groups, allowing relative quantification of multiple samples in one measurement. Here we report a new isobaric labelling reagent, where the balancer and the reporter are linked by a sulfoxide group, which, based on the sulfoxide pyrolysis, leads to easy and asymmetric cleavage at low fragmentation energy. The fragmentation of our new design is significantly improved, yielding more intense complementary ion signals, allowing complementary ion cluster analysis as well.
现代蛋白质组学需要试剂来精确定量复杂混合物中的肽。肽标记最典型的方法是使用等重标记物,它由平衡部分和报告部分组成,在气相中分离。巧妙的稳定同位素分布提供了具有相同分子量但报告基团质量不同的多种试剂,允许在一次测量中对多个样本进行相对定量。在这里,我们报告了一种新的等重标记试剂,其中平衡部分和报告部分通过亚砜基连接,基于亚砜基的热解,在低碎片化能量下导致容易和不对称的切割。我们新设计的碎片化得到了显著改善,产生了更强烈的互补离子信号,允许进行互补离子簇分析。