首页> 外文会议>American Society for Mass Spectrometry Conference on Mass Spectrometry and Allied Topics >'Mapping the HEPG2 Lipidome as effected by Niacin using Products of All Acquisition on an new generation Q Q TOF'
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'Mapping the HEPG2 Lipidome as effected by Niacin using Products of All Acquisition on an new generation Q Q TOF'

机译:“将HepG2脂质体映射,使用烟酸的所有采集产品对新一代Q Q TOF进行了影响”

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Recent developments in instrumentation and software have made it possible to acquire an array of data that can be mined for information of interest as opposed to designing an experiment to capture it directly. Data collected in an untargeted manner was mined for both expected and unexpected changes in the lipidome caused by niacin as reflected by the incorporation of a stable isotope label. An equivalent experiment using conventional acquisition methods was not possible. To demonstrate this new paradigm, HEPG2 cells were grown in the presence and absence of a stable labeled fatty acid and with and without the presence of niacin to observe the flux of the label into the various lipid pathways. Data were acquire on the Sciex TripleTOF 5600 using a scan function where precursor masses are iterated in 1 amu increments from m/z 200 to m/z 1000. Given the speed of the TOF it was possible to acquire ms/ms spectra for all 800 precursor ions in just under 3 minutes where each spectrum is the average of approximately 18 scans/precursor mass. All data were acquired using unit mass resolution for the precursor mass and approximately 40000 resolution of the product ion spectra, with collision energy ramping for each m/z event.
机译:在仪器和软件的最新发展使人们有可能获得可开采感兴趣的信息,而不是设计一个实验来直接获取其数据数组。在一个非靶向方式收集到的数据被开采引起的烟酸既脂质组预期和非预期的变化通过一个稳定的同位素标记的掺入所反映的。使用常规的采集方法的等效实验是不可能的。为了证明这一新的模式,HepG2细胞以稳定的标记的脂肪酸的存在和不存在,并具有和不烟酸到标签的通量观察到各种脂质途径的存在下生长。使用扫描功能,其中的前体质量块在从M / Z 200 1个AMU增量到m迭代数据分别对的Sciex的TripleTOF 5600获取/ Z 1000鉴于TOF它是能够获取MS的速度/ MS谱对所有800前体离子中只是在3分钟内,其中每个光谱是约18次/前体的质量的平均值。所有数据使用为所述前体质量单位质量分辨率和大约40000分辨率产物离子质谱获取的,以及每个M / Z事件碰撞能量斜坡。

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