Cedra Corp., Austin, TX, USA. [corrected]
Rapid Commun Mass Spectrom. 2010 Sep;24(18):2730-4. doi: 10.1002/rcm.4702.
Increases in the study of protein-metal complexes, as well as in metal displacement in protein-metal complexes under native conditions for optimum catalytic properties in drug research and catalyst design, demands a separation/detection technology that can accurately measure metal displacement and stoichiometry in protein-metal complexes. Both nuclear magnetic resonance (NMR) and X-ray diffraction techniques have been used for this purpose; however, these techniques lack sensitivity. Electrospray ionization mass spectrometry (ESI-MS) using direct infusion offers higher sensitivity than the former techniques and provides molecular distribution of various protein-metal complexes. However, since protein-metal complexes under native conditions usually are dissolved in salt solutions, their direct ESI-MS analysis requires off-line sample clean-up prior to MS analysis to avoid sample suppression during ESI. Moreover, direct infusion of the salty solution promotes non-specific salt adduct formation by the protein-metal complexes under ESI-MS, which complicates the identification and stoichiometry measurements of the protein-metal complexes. Because of the high mass of protein-metal complexes and lack of sufficient resolution by most mass spectrometers to separate non-specific from specific metal-protein complexes, accurate protein-metal stoichiometry measurements require some form of sample clean up prior to ESI-MS analysis. In this study, we demonstrate that capillary electrophoresis/electrospray ionization in conjunction with a medium-resolution (approximately 10,000) mass spectrometer is an efficient and fast method for the measurement of the stoichiometry of the protein-metal complexes under physiological conditions (pH approximately 7). The metal displacement of Co(2+) to Cd(2+), two metal ions necessary for activation in the monomeric AHL lactonase produced by B. thuringiensis, has been used as a proof of concept.
在研究蛋白质-金属复合物方面的研究不断增加,以及在生理条件下研究蛋白质-金属复合物中金属的置换,以优化药物研究和催化剂设计中的最佳催化性能,这都需要一种分离/检测技术,能够准确测量蛋白质-金属复合物中的金属置换和化学计量。为此,已经使用了核磁共振(NMR)和 X 射线衍射技术;然而,这些技术缺乏灵敏度。使用直接注入的电喷雾电离质谱(ESI-MS)比前两种技术具有更高的灵敏度,并提供了各种蛋白质-金属复合物的分子分布。然而,由于生理条件下的蛋白质-金属复合物通常溶解在盐溶液中,它们的直接 ESI-MS 分析需要在 MS 分析之前进行离线样品净化,以避免 ESI 过程中的样品抑制。此外,盐溶液的直接注入会促进蛋白质-金属复合物在 ESI-MS 下形成非特异性盐加合物,这使得蛋白质-金属复合物的鉴定和化学计量测量变得复杂。由于蛋白质-金属复合物的分子量较高,并且大多数质谱仪的分辨率不足以分离非特异性和特异性的金属-蛋白质复合物,因此,准确的蛋白质-金属化学计量测量需要在 ESI-MS 分析之前进行某种形式的样品净化。在本研究中,我们证明了毛细管电泳/电喷雾电离与中分辨率(约 10000)质谱仪相结合,是一种在生理条件下(pH 约 7)测量蛋白质-金属复合物化学计量的有效且快速的方法。已经使用 Co(2+)到 Cd(2+)的金属置换,即苏云金芽孢杆菌产生的单体 AHL 内酯酶所需的两种激活金属离子,作为概念验证。