Butler Karen E, Takinami Yoshihiko, Rainczuk Adam, Baker Erin S, Roberts Blaine R
Department of Chemistry, North Carolina State University, Raleigh, NC, United States.
Bruker Japan K.K., Yokohama City, Japan.
Front Chem. 2021 Feb 9;9:614595. doi: 10.3389/fchem.2021.614595. eCollection 2021.
Native mass spectrometry has emerged as a powerful tool for structural biology as it enables the evaluation of molecules as they occur in their physiological conditions. Ion mobility spectrometry-mass spectrometry (IMS-MS) has shown essential in these analyses as it allows the measurement of the shape of a molecule, denoted as its collision cross section (CCS), and mass. The structural information garnered from native IMS-MS provides insight into the tertiary and quaternary structure of proteins and can be used to validate NMR or crystallographic X-ray structures. Additionally, due to the rapid nature (millisecond measurements) and ability of IMS-MS to analyze heterogeneous solutions, it can be used to address structural questions not possible with traditional structural approaches. Herein, we applied multiple solution conditions to systematically denature bovine Cu/Zn-superoxide dismutase (SOD1) and assess its unfolding pathway from the holo-dimer to the holo-monomer, single-metal monomer, and apo-monomer. Additionally, we compared and noted 1-2% agreement between CCS values from both drift tube IMS and trapped IMS for the SOD1 holo-monomer and holo-dimer. The observed CCS values were in excellent agreement with computational CCS values predicted from the homo-dimer crystal structure, showcasing the ability to use both IMS-MS platforms to provide valuable structural information for molecular modeling of protein interactions and structural assessments.
原生质谱已成为结构生物学的一种强大工具,因为它能够在分子处于生理条件下时对其进行评估。离子淌度谱-质谱联用(IMS-MS)在这些分析中已显示出至关重要的作用,因为它能够测量分子的形状(用其碰撞截面(CCS)表示)和质量。从原生IMS-MS获得的结构信息为蛋白质的三级和四级结构提供了深入了解,并且可用于验证核磁共振(NMR)或晶体学X射线结构。此外,由于IMS-MS具有快速的特性(毫秒级测量)以及能够分析异质溶液的能力,它可用于解决传统结构方法无法解决的结构问题。在此,我们应用多种溶液条件来系统地使牛铜锌超氧化物歧化酶(SOD1)变性,并评估其从全酶二聚体到全酶单体、单金属单体和脱辅基单体的解折叠途径。此外,我们比较并注意到对于SOD1全酶单体和全酶二聚体,漂移管IMS和阱式IMS的CCS值之间有1-2%的一致性。观察到的CCS值与从同二聚体晶体结构预测的计算CCS值非常吻合,展示了使用这两种IMS-MS平台为蛋白质相互作用的分子建模和结构评估提供有价值结构信息的能力。