Department of Proteomics and Signal Transduction, Max-Planck Institute for Biochemistry, Am Klopferspitz 18, D-82152 Martinsried, Germany.
Mol Cell Proteomics. 2012 Mar;11(3):O111.013698. doi: 10.1074/mcp.O111.013698. Epub 2011 Dec 9.
Although only a few years old, the combination of a linear ion trap with an Orbitrap analyzer has become one of the standard mass spectrometers to characterize proteins and proteomes. Here we describe a novel version of this instrument family, the Orbitrap Elite, which is improved in three main areas. The ion transfer optics has an ion path that blocks the line of sight to achieve more robust operation. The tandem MS acquisition speed of the dual cell linear ion trap now exceeds 12 Hz. Most importantly, the resolving power of the Orbitrap analyzer has been increased twofold for the same transient length by employing a compact, high-field Orbitrap analyzer that almost doubles the observed frequencies. An enhanced Fourier Transform algorithm-incorporating phase information-further doubles the resolving power to 240,000 at m/z 400 for a 768 ms transient. For top-down experiments, we combine a survey scan with a selected ion monitoring scan of the charge state of the protein to be fragmented and with several HCD microscans. Despite the 120,000 resolving power for SIM and HCD scans, the total cycle time is within several seconds and therefore suitable for liquid chromatography tandem MS. For bottom-up proteomics, we combined survey scans at 240,000 resolving power with data-dependent collision-induced dissociation of the 20 most abundant precursors in a total cycle time of 2.5 s-increasing protein identifications in complex mixtures by about 30%. The speed of the Orbitrap Elite furthermore allows scan modes in which complementary dissociation mechanisms are routinely obtained of all fragmented peptides.
尽管线性离子阱与轨道阱分析器的组合仅有几年的历史,但它已经成为用于鉴定蛋白质和蛋白质组的标准质谱仪之一。在这里,我们描述了该仪器系列的一个新版本,即 Orbitrap Elite,它在三个主要方面得到了改进。离子传输光学器件具有一条阻挡视线的离子路径,从而实现更稳健的操作。双池线性离子阱的串联 MS 采集速度现在超过了 12 Hz。最重要的是,通过采用紧凑型高场轨道阱分析器,将轨道阱分析器的分辨率提高了一倍,而对于相同的瞬变长度,观察到的频率几乎增加了一倍。增强的傅里叶变换算法(结合相位信息)将分辨率进一步提高到 240,000,在 m/z 400 时的瞬变时间为 768 ms。对于自上而下的实验,我们将蛋白质的总离子流扫描与所选择的离子监测扫描以及几个 HCD 微扫描相结合。尽管 SIM 和 HCD 扫描的分辨率为 120,000,但总循环时间在几秒钟内,因此适用于液相色谱串联质谱。对于自下而上的蛋白质组学,我们将 240,000 分辨率的总离子流扫描与 2.5 秒内 20 种最丰富前体的全循环时间内的数据依赖性碰撞诱导解离相结合,在复杂混合物中增加了约 30%的蛋白质鉴定。Orbitrap Elite 的速度还允许获得所有碎片化肽的互补解离机制的扫描模式。