He Muyi, Luo Pan, Hong Jie, Wang Xiaofeng, Wu Haimei, Zhang Rongkai, Qu Feng, Xiang Ye, Xu Wei
College of Information Science, Shenzhen University, Shenzhen 518060, China.
School of Life Science, Beijing Institute of Technology, Beijing 100081, China.
ACS Omega. 2019 Jan 31;4(1):2377-2386. doi: 10.1021/acsomega.8b03224.
The 3D structures of biomolecules determine their biological function. Established methods in biomolecule structure determination typically require purification, crystallization, or modification of target molecules, which limits their applications for analyzing trace amounts of biomolecules in complex matrices. Here, we developed instruments and methods of mobility capillary electrophoresis (MCE) and its coupling with MS for the 3D structural analysis of biomolecules in the liquid phase. Biomolecules in complex matrices could be separated by MCE and sequentially detected by MS. The effective radius and the aspect ratio of each separated biomolecule were simultaneously determined through the separation by MCE, which were then used as restraints in determining biomolecule conformations through modeling. Feasibility of this method was verified by analyzing a mixture of somatostatin and bradykinin, two peptides with known liquid-phase structures. Proteins could also be structurally analyzed using this method, which was demonstrated for lysozyme. The combination of MCE and MS for complex sample analysis was also demonstrated. MCE and MCE-MS would allow us to analyze trace amounts of biomolecules in complex matrices, which has the potential to be an alternative and powerful biomolecule structure analysis technique.
生物分子的三维结构决定其生物学功能。生物分子结构测定的现有方法通常需要对目标分子进行纯化、结晶或修饰,这限制了它们在分析复杂基质中痕量生物分子方面的应用。在此,我们开发了流动毛细管电泳(MCE)及其与质谱联用的仪器和方法,用于液相中生物分子的三维结构分析。复杂基质中的生物分子可通过MCE分离并依次由质谱检测。通过MCE分离同时确定每个分离生物分子的有效半径和长宽比,然后将其用作通过建模确定生物分子构象的约束条件。通过分析生长抑素和缓激肽(两种具有已知液相结构的肽)的混合物验证了该方法的可行性。该方法也可用于蛋白质的结构分析,以溶菌酶为例进行了证明。还展示了MCE和MCE-MS用于复杂样品分析的情况。MCE和MCE-MS将使我们能够分析复杂基质中的痕量生物分子,这有可能成为一种替代且强大的生物分子结构分析技术。