Laser microdissection and atmospheric pressure chemical ionization mass spectrometry coupled for multimodal imaging

Matthias Lorenz, Olga S. Ovchinnikova, Vilmos Kertesz, Gary J. Van Berkel

Research output: Contribution to journalArticlepeer-review

30 Scopus citations

Abstract

RATIONALE Improvement in spatial resolution of atmospheric pressure molecular chemical imaging is required to resolve distinct surface features in the low micrometer and sub-micrometer scale. Laser capture microdissection systems have the capability to focus laser light to a few micrometers. This type of system, when employed for laser ablation (LA) mass spectrometry (MS)-based chemical imaging, has the potential to achieve high spatial resolution with multimodal optical and chemical imaging capability. METHODS A commercially available laser capture microdissection system was coupled to a modified ion source of a mass spectrometer. This design allowed for sampling of laser-ablated material via a transfer tube directly into the ionization region. Ionization of the ablated material was accomplished using atmospheric pressure chemical ionization (APCI). RESULTS Rhodamine 6G dye of red permanent marker ink in a laser etched pattern as well as cholesterol and phosphatidylcholine in a cerebellum mouse brain thin tissue section were identified and imaged from the mass spectral data. Employing a spot diameter of 8 μm using the 10× microscope cutting objective and lateral oversampling resulted in a pixel size of about 3.7 μm in the same dimension. Distinguishing between features approximately 13 μm apart in a cerebellum mouse brain thin tissue section was demonstrated in a multimodal fashion co-registering optical and mass spectral images. CONCLUSIONS A LA/APCI-MS system was developed that comprised a commercially available laser microdissection instrument for transmission geometry LA and a modestly modified ion source for secondary ionization of the ablated material. The set-up was successfully applied for multimodal imaging using the ability to co-register bright field, fluorescence and mass spectral chemical images on one platform. Published in 2013. This article is a US Government work and is in the public domain in the USA.

Original languageEnglish
Pages (from-to)1429-1436
Number of pages8
JournalRapid Communications in Mass Spectrometry
Volume27
Issue number13
DOIs
StatePublished - Jul 15 2013

Fingerprint

Dive into the research topics of 'Laser microdissection and atmospheric pressure chemical ionization mass spectrometry coupled for multimodal imaging'. Together they form a unique fingerprint.

Cite this