Walko Martin, Hewitt Eric, Radford Sheena E, Wilson Andrew J
School of Chemistry, University of Leeds Leeds LS2 9JT UK
Astbury Centre for Structural Molecular Biology, University of Leeds Leeds LS2 9JT UK.
RSC Adv. 2019 Mar 7;9(14):7610-7614. doi: 10.1039/c8ra10436k. eCollection 2019 Mar 6.
Chemical cross-linking mass-spectrometry (XL-MS) represents a powerful methodology to map ligand/biomacromolecule interactions, particularly where conventional methods such as X-ray crystallography, nuclear magnetic resonance (NMR) spectroscopy or cryo-electron microscopy (EM) are not feasible. In this manuscript, we describe the design and synthesis of two new photo-crosslinking reagents that can be used to specifically label free thiols through either maleimido or methanethiosulfonate groups and facilitate PXL-MS workflows. Both crosslinkers are based on light sensitive diazirines - precursors of highly reactive carbenes which offer additional advantages over alternative crosslinking groups such as benzophenones and aryl nitrenes given the controlled rapid and more indiscriminate reactivity.
化学交联质谱法(XL-MS)是一种强大的方法,可用于绘制配体/生物大分子相互作用图谱,特别是在诸如X射线晶体学、核磁共振(NMR)光谱或冷冻电子显微镜(EM)等传统方法不可行的情况下。在本手稿中,我们描述了两种新型光交联试剂的设计与合成,它们可通过马来酰亚胺基或甲硫基磺酸盐基团特异性标记游离硫醇,并促进PXL-MS工作流程。两种交联剂均基于对光敏感的重氮丙啶——高活性卡宾的前体,与诸如二苯甲酮和芳基氮烯等其他交联基团相比,鉴于其可控的快速且更具普遍性的反应性,具有额外的优势。