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

dc.citation.epage6736en_US
dc.citation.issue22en_US
dc.citation.spage6732en_US
dc.citation.volume138en_US
dc.citation.woscount5
dc.contributor.authorFagerer, Stephan R.en_US
dc.contributor.authorSchmid, Thomasen_US
dc.contributor.authorIbanez, Alfredo J.en_US
dc.contributor.authorPabst, Martinen_US
dc.contributor.authorSteinhoff, Roberten_US
dc.contributor.authorJefimovs, Konstantinsen_US
dc.contributor.authorUrban, Pawel L.en_US
dc.contributor.authorZenobi, Renatoen_US
dc.contributor.department交大名義發表zh_TW
dc.contributor.departmentNational Chiao Tung Universityen_US
dc.date.accessioned2014-12-08T15:32:46Z
dc.date.available2014-12-08T15:32:46Z
dc.date.issued2013en_US
dc.description.abstractIn 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 beta-carotene, the precursor of astaxanthin, into the cytosol.en_US
dc.identifier.doi10.1039/c3an01135fen_US
dc.identifier.issn0003-2654en_US
dc.identifier.journalANALYSTen_US
dc.identifier.urihttp://dx.doi.org/10.1039/c3an01135fen_US
dc.identifier.urihttps://ir.lib.nycu.edu.tw/handle/11536/22904
dc.identifier.wosnumberWOS:000325819300004
dc.language.isoen_USen_US
dc.titleAnalysis of single algal cells by combining mass spectrometry with Raman and fluorescence mappingen_US
dc.typeArticleen_US

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