Syka John E P, Marto Jarrod A, Bai Dina L, Horning Stevan, Senko Michael W, Schwartz Jae C, Ueberheide Beatrix, Garcia Benjamin, Busby Scott, Muratore Tara, Shabanowitz Jeffrey, Hunt Donald F
Engineering Physics Program, University of Virginia, Charlottesville, Virginia 22901, USA.
J Proteome Res. 2004 May-Jun;3(3):621-6. doi: 10.1021/pr0499794.
We describe the design and performance of a prototype high performance hybrid mass spectrometer. This instrument consists of a linear quadrupole ion trap (QLT) coupled to a Fourier transform ion cyclotron resonance mass analyzer (FTMS). This configuration provides rapid and automated MS and MS/MS analyses, similar to the "data dependent scanning" found on standard 3-D Paul traps, but with substantially improved internal scan dynamic range, mass measurement accuracy, mass resolution, and detection limits. Sequence analysis of peptides at the zeptomole level is described. The recently released, commercial version of this instrument operates in the LC/MS mode (1 s/scan) with a mass resolution of 100 000 and is equipped with automatic gain control to provide mass measurement accuracy of 1-2 ppm without internal standard. Methodology is described that uses this instrument to compare the post-translational modifications present on histone H3 isolated from asynchronously growing cells and cells arrested in mitosis.
我们描述了一种高性能混合质谱仪原型的设计与性能。该仪器由一个与傅里叶变换离子回旋共振质量分析仪(FTMS)相连的线性四极杆离子阱(QLT)组成。这种配置提供了快速且自动化的质谱和串联质谱分析,类似于标准三维保罗阱上的“数据依赖扫描”,但内部扫描动态范围、质量测量精度、质量分辨率和检测限都有显著提高。文中描述了在zeptomole水平对肽段进行序列分析的情况。该仪器最近发布的商业版本以液相色谱/质谱模式(1秒/扫描)运行,质量分辨率为100000,并且配备了自动增益控制,无需内标即可提供1 - 2 ppm的质量测量精度。文中还描述了使用该仪器比较从异步生长细胞和有丝分裂停滞细胞中分离出的组蛋白H3上存在的翻译后修饰的方法。