Analysis of single algal cells by combining mass spectrometry with Raman and fluorescence mapping

Journal Article (2013)
Authors

Stephan R. Fagerer (ETH Zürich)

Thomas Schmid (ETH Zürich)

Alfredo J. Ibáñez (ETH Zürich)

Martin Pabst (ETH Zürich)

Robert F. Steinhoff (ETH Zürich)

Konstantins Jefimovs (Swiss Federal Laboratories for Materials Science and Technology (Empa))

Pawel L. Urban (National Chiao Tung University Taiwan)

Renato Zenobi (ETH Zürich)

Affiliation
External organisation
To reference this document use:
https://doi.org/10.1039/c3an01135f
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Publication Year
2013
Language
English
Affiliation
External organisation
Issue number
22
Volume number
138
Pages (from-to)
6732-6736
DOI:
https://doi.org/10.1039/c3an01135f

Abstract

In order to investigate metabolic properties of single cells of freshwater algae (Haematococcus pluvialis), we implement matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) in combination with microspectroscopic mapping. Straightforward coupling of these two detection platforms was possible thanks to the self-aliquoting properties of micro-arrays for mass spectrometry (MAMS). Following Raman and fluorescence imaging, the isolated cells were covered with a MALDI matrix for targeted metabolic analysis by MALDI-MS. The three consecutive measurements carried out on the same cells yielded complementary information. Using this method, we were able to study the encystment of H. pluvialis-by monitoring the adenosine triphosphate (ATP) to adenosine diphosphate (ADP) ratio during the build-up of astaxanthin in the cells as well as the release of β-carotene, the precursor of astaxanthin, into the cytosol.

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