http://www.cnr.it/ontology/cnr/individuo/prodotto/ID322450
Chemical aspects of the primary ionization mechanisms in matrix-assisted laser desorption ionization (Articolo in rivista)
- Type
- Label
- Chemical aspects of the primary ionization mechanisms in matrix-assisted laser desorption ionization (Articolo in rivista) (literal)
- Anno
- 2014-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1255/ejms.1296 (literal)
- Alternative label
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Molin L.; Crotti S.; Seraglia R.; Czarnocki Z.; Szawka?o J.; Maurin J. K.; Pluci?ski F. A.; Traldi P. (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
- https://www.impublications.com/content/abstract?code=E20_0437 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- 1,3,8 :National Council of Researches, Institute for Energetics and Interphases, Corso Stati Uniti 4, 35100 Padua, Italy /
2 : Experimental and Clinical Pharmacology Unit, Centro di Riferimento Oncologico - National Cancer Institute, Aviano PN, Italy /
4,5 : Faculty of Chemistry, University of Warsaw, Pasteura 1, 02-093 Warsaw, Poland /
6,7 : National Medicines Institute, Che?mska 30/34, 00-725 Warsaw, Poland /
6,7 : National Centre for Nuclear Research, 05-400 Otwock, ?wierk, Poland (literal)
- Titolo
- Chemical aspects of the primary ionization mechanisms in matrix-assisted laser desorption ionization (literal)
- Abstract
- It has been proposed that the primary ionization mechanism occurring in matrix-assisted laser desorption ionization (MALDI) experi-ments originates from the presence, in the solid-state matrix-analytes sample, of matrix dimers. These species are formed by the interaction of carboxylic groups present in the matrix molecules with the formation of strong hydrogen bonds. Theoretical calculations proved that the laser irradiation of these structures leads to one or two H-bridge cleavages, giving rise to an \"open\" dimer structure or to disproportionation with the formation of MH+ and [M - H]- species. The ions so formed can be considered highly effective in their reac¬tion with analyte ions, leading to their protonation (or deprotonation). To achieve further evidence for these proposals, in the present study the energetics of the reactions of ions from different aromatic carboxylic acids with two amino acids (glycine and lysine) and three multipeptides (gly-gly, gly-gly-gly and gly-gly-gly-gly) was investigated. The lowest ?G values were obtained for 2,5-dihydroxybenzoic acid, widely employed as the MALDI matrix. Also, for p-nitrobenzoic acid the reaction is slightly exothermic, while for the other aromatic carboxylic acids derivatives positives values of ?G are present. (literal)
- Prodotto di
- Autore CNR
- Insieme di parole chiave
Incoming links:
- Prodotto
- Autore CNR di
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#rivistaDi
- Insieme di parole chiave di