Zavalin Andre, Todd Erik M, Rawhouser Patrick D, Yang Junhai, Norris Jeremy L, Caprioli Richard M
J Mass Spectrom. 2012 Nov;47(11):i. doi: 10.1002/jms.3132.
Discussions about MALDI imaging frequently turn to the topic of spatial resolution and the eff orts of some researchers in the field to push towards routine imaging of tissue sections at a cellular scale. Some factors that limit resolution are, the size of the focused desorption laser beam and analyte delocalization from the solution-based sample preparation. With solvent-free matrix application techniques analyte delocalization is less of a concern and the size of the focused laser is the major limiter of spatial resolution. In the Special Feature, Professor Caprioli and co-workers at Vanderbilt University demonstrate a new instrumental approach for improving spatial resolution. They have modifi ed a MALDI-TOF system to use transmission-mode geometry, in which the desorption laser is focused onto the matrix crystals from behind and through the target and sample rather than conventional front-side illumination where the laser is focused onto the crystals directly. They show that by moving the laser source behind the sample target, they can optimize the laser focus to achieve cellular resolution for MALDI imaging.
关于基质辅助激光解吸电离成像(MALDI成像)的讨论常常会转向空间分辨率这一话题,以及该领域一些研究人员为推动在细胞尺度上对组织切片进行常规成像所做的努力。一些限制分辨率的因素包括聚焦解吸激光束的大小以及基于溶液的样品制备过程中分析物的离域现象。采用无溶剂基质应用技术时,分析物离域问题就不那么令人担忧了,而聚焦激光的大小则是空间分辨率的主要限制因素。在本期专题文章中,范德堡大学的卡普里奥利教授及其同事展示了一种提高空间分辨率的新仪器方法。他们对一台基质辅助激光解吸电离飞行时间(MALDI-TOF)系统进行了改进,使其采用透射模式几何结构,即解吸激光从样品靶材后方穿过靶材和样品聚焦到基质晶体上,而不是像传统的正面照明那样将激光直接聚焦到晶体上。他们表明,通过将激光源移到样品靶材后方,可以优化激光聚焦,从而实现MALDI成像的细胞分辨率。