Römpp Andreas, Both Jean-Pierre, Brunelle Alain, Heeren Ron M A, Laprévote Olivier, Prideaux Brendan, Seyer Alexandre, Spengler Bernhard, Stoeckli Markus, Smith Donald F
Institute of Inorganic and Analytical Chemistry, Justus Liebig University, Schubertstrasse 60, Bldg. 16, 35392, Giessen, Germany,
Anal Bioanal Chem. 2015 Mar;407(8):2329-35. doi: 10.1007/s00216-014-8410-7. Epub 2015 Jan 10.
Mass spectrometry imaging has become a popular tool for probing the chemical complexity of biological surfaces. This led to the development of a wide range of instrumentation and preparation protocols. It is thus desirable to evaluate and compare the data output from different methodologies and mass spectrometers. Here, we present an approach for the comparison of mass spectrometry imaging data from different laboratories (often referred to as multicenter studies). This is exemplified by the analysis of mouse brain sections in five laboratories in Europe and the USA. The instrumentation includes matrix-assisted laser desorption/ionization (MALDI)-time-of-flight (TOF), MALDI-QTOF, MALDI-Fourier transform ion cyclotron resonance (FTICR), atmospheric-pressure (AP)-MALDI-Orbitrap, and cluster TOF-secondary ion mass spectrometry (SIMS). Experimental parameters such as measurement speed, imaging bin width, and mass spectrometric parameters are discussed. All datasets were converted to the standard data format imzML and displayed in a common open-source software with identical parameters for visualization, which facilitates direct comparison of MS images. The imzML conversion also allowed exchange of fully functional MS imaging datasets between the different laboratories. The experiments ranged from overview measurements of the full mouse brain to detailed analysis of smaller features (depending on spatial resolution settings), but common histological features such as the corpus callosum were visible in all measurements. High spatial resolution measurements of AP-MALDI-Orbitrap and TOF-SIMS showed comparable structures in the low-micrometer range. We discuss general considerations for planning and performing multicenter studies in mass spectrometry imaging. This includes details on the selection, distribution, and preparation of tissue samples as well as on data handling. Such multicenter studies in combination with ongoing activities for reporting guidelines, a common data format (imzML) and a public data repository can contribute to more reliability and transparency of MS imaging studies.
质谱成像已成为探究生物表面化学复杂性的常用工具。这促使了一系列仪器设备和制备方案的发展。因此,评估和比较不同方法及质谱仪的数据输出很有必要。在此,我们提出一种比较来自不同实验室的质谱成像数据的方法(通常称为多中心研究)。以欧洲和美国五个实验室对小鼠脑切片的分析为例。所使用的仪器包括基质辅助激光解吸/电离(MALDI)-飞行时间(TOF)质谱仪、MALDI-四极杆飞行时间(QTOF)质谱仪、MALDI-傅里叶变换离子回旋共振(FTICR)质谱仪、大气压(AP)-MALDI-轨道阱质谱仪以及簇射TOF-二次离子质谱(SIMS)仪。文中讨论了诸如测量速度、成像像素宽度和质谱参数等实验参数。所有数据集都被转换为标准数据格式imzML,并在具有相同可视化参数的通用开源软件中显示,这便于直接比较质谱图像。imzML转换还允许在不同实验室之间交换功能完整的质谱成像数据集。实验范围从对整个小鼠脑的概述测量到对较小特征的详细分析(取决于空间分辨率设置),但所有测量中都能看到诸如胼胝体等常见组织学特征。AP-MALDI-轨道阱质谱仪和TOF-SIMS的高空间分辨率测量在低微米范围内显示出可比的结构。我们讨论了质谱成像中规划和开展多中心研究的一般注意事项。这包括组织样本的选择、分配和制备以及数据处理的详细信息。这种多中心研究与正在进行的报告指南活动、通用数据格式(imzML)和公共数据存储库相结合,可有助于提高质谱成像研究的可靠性和透明度。