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pubmed-article:17260136rdf:typepubmed:Citationlld:pubmed
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pubmed-article:17260136pubmed:issue5lld:pubmed
pubmed-article:17260136pubmed:dateCreated2007-2-20lld:pubmed
pubmed-article:17260136pubmed:abstractTextApplication of matrix-assisted laser-desorption ionization mass spectrometry (MALDI-MS) to small-molecule detection is often limited, because of high matrix background signals in the low-mass region. We report here an approach in which a mixture of two conventional MALDI matrices with different proton affinity was used to suppress the formation of matrix clusters and fragments. Specifically, when acidic alpha-cyano-4-hydroxycinnamic acid (CHCA) and basic 9-aminoacridine (9-AA) were used as the binary matrix, fewer background matrix peaks were observed in both positive and negative-mode detection of small molecules. In addition, the presence of CHCA substantially reduced the laser fluence needed for analyte desorption and ionization; thus better signal-to-background ratios were observed for negatively charged inositol phosphates in complex plant extracts.lld:pubmed
pubmed-article:17260136pubmed:languageenglld:pubmed
pubmed-article:17260136pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:17260136pubmed:statusPubMed-not-MEDLINElld:pubmed
pubmed-article:17260136pubmed:monthMarlld:pubmed
pubmed-article:17260136pubmed:issn1618-2642lld:pubmed
pubmed-article:17260136pubmed:authorpubmed-author:HeLinLlld:pubmed
pubmed-article:17260136pubmed:authorpubmed-author:GuoZhongZlld:pubmed
pubmed-article:17260136pubmed:issnTypePrintlld:pubmed
pubmed-article:17260136pubmed:volume387lld:pubmed
pubmed-article:17260136pubmed:ownerNLMlld:pubmed
pubmed-article:17260136pubmed:authorsCompleteYlld:pubmed
pubmed-article:17260136pubmed:pagination1939-44lld:pubmed
pubmed-article:17260136pubmed:year2007lld:pubmed
pubmed-article:17260136pubmed:articleTitleA binary matrix for background suppression in MALDI-MS of small molecules.lld:pubmed
pubmed-article:17260136pubmed:affiliationDepartment of Chemistry, North Carolina State University, Raleigh, NC 27695, USA.lld:pubmed
pubmed-article:17260136pubmed:publicationTypeJournal Articlelld:pubmed
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