| Literature DB >> 30456596 |
Antonín Bednařík1,2, Markéta Machálková1, Eugene Moskovets3, Kateřina Coufalíková1, Pavel Krásenský1, Pavel Houška4, Jiří Kroupa4, Jarmila Navrátilová5,6, Jan Šmarda5, Jan Preisler7,8.
Abstract
The practicality of matrix-assisted laser desorption/ionization (MALDI) time-of-flight (TOF) mass spectrometry (MS) applied to molecular imaging of biological tissues is limited by the analysis speed. Typically, a relatively low speed of stop-and-go micromotion of XY stages is considered as a factor substantially reducing the rate with which fresh sample material can be supplied to the laser spot. The sample scan rate in our laboratory-built high-throughput imaging TOF mass spectrometer was significantly improved through the use of a galvanometer-based optical scanner performing fast laser spot repositioning on a target plate. The optical system incorporated into the ion source of our MALDI TOF mass spectrometer allowed focusing the laser beam via a modified grid into a 10-μm round spot. This permitted the acquisition of high-resolution MS images with a well-defined pixel size at acquisition rates exceeding 100 pixel/s. The influence of selected parameters on the total MS imaging time is discussed. The new scanning technique was employed to display the distribution of an antitumor agent in 3D colorectal adenocarcinoma cell aggregates; a single MS image comprising 100 × 100 pixels with 10-μm lateral resolution was recorded in approximately 70 s. Graphical Abstract.Entities:
Keywords: 3D cell aggregates; Colorectal adenocarcinoma; Grid ion source; High throughput; Laser beam scanning; MALDI; MSI; Mass spectrometry imaging; Spheroids; TOF
Mesh:
Year: 2018 PMID: 30456596 DOI: 10.1007/s13361-018-2078-8
Source DB: PubMed Journal: J Am Soc Mass Spectrom ISSN: 1044-0305 Impact factor: 3.109