Department of Pharmaceutical Chemistry & Bioanalytics, Institute of Pharmacy, Martin-Luther University Halle-Wittenberg, D-06120 Halle (Saale), Germany.
Rapid Commun Mass Spectrom. 2011 Jan 15;25(1):155-61. doi: 10.1002/rcm.4812.
The concept of protein cross-linking in combination with mass spectrometry holds great promise to derive structural information on protein conformation and protein-protein interactions. We recently presented a dissociative amine-reactive cross-linker (NHS-BuUrBu-NHS) that is shown herein to be universally applicable to protein structure analysis under matrix-assisted laser desorption/ionization tandem mass spectrometric (MALDI-MS/MS) conditions, based on the examples of the peptides substance P, luteinizing hormone releasing hormone (LHRH), and the 32-kDa ligand-binding domain of peroxisome proliferator-activated receptor alpha (PPARα). The characteristic fragment ion patterns and constant neutral losses of the cross-linker greatly simplify the identification of different cross-linked species from complex mixtures and drastically reduce the potential of identifying false-positive cross-links. Therefore, this cross-linker holds an enormous potential for deriving structural information of proteins and protein complexes in a highly automated fashion.
蛋白质交联与质谱联用的概念为获取蛋白质构象和蛋白质-蛋白质相互作用的结构信息提供了巨大的潜力。我们最近提出了一种解离胺反应交联剂(NHS-BuUrBu-NHS),本文通过对多肽 P 物质、促黄体激素释放激素(LHRH)和过氧化物酶体增殖物激活受体α(PPARα)的 32kDa 配体结合域的示例,证明了该交联剂在基质辅助激光解吸/电离串联质谱(MALDI-MS/MS)条件下普遍适用于蛋白质结构分析。交联剂的特征片段离子模式和恒定的中性损失极大地简化了从复杂混合物中鉴定不同交联物种的过程,并大大降低了鉴定假阳性交联的可能性。因此,该交联剂具有以高度自动化方式获取蛋白质和蛋白质复合物结构信息的巨大潜力。