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dc.contributor.authorMarcos, Josep
dc.contributor.authorIbáñez, Maria
dc.contributor.authorVentura, Rosa
dc.contributor.authorSegura, Jordi
dc.contributor.authorTo-Figueras, Jordi
dc.contributor.authorPozo, Oscar J.
dc.date.accessioned2016-07-15T11:43:21Z
dc.date.available2016-07-15T11:43:21Z
dc.date.issued2015-07
dc.identifier.citationMARCOS, Josep, et al. Mass spectrometric characterisation of a condensation product between porphobilinogen and indolyl‐3‐acryloylglycine in urine of patients with acute intermittent porphyria. Journal of Mass Spectrometry, 2015, vol. 50, no 7, p. 929-937.ca_CA
dc.identifier.urihttp://hdl.handle.net/10234/161732
dc.description.abstractWe document the presence of a previously unknown species in the urine of patients with acute intermittent porphyria (AIP). The compound was fully characterised by liquid chromatography tandem mass spectrometry. Interpretation of both full spectrum acquisition and product ion spectra acquired in positive and negative ionisation modes by quadrupole time of flight MS allowed for the identification of a condensation product arising from porphobilinogen (PBG, increased in the urine of AIP patients) and indolyl-3-acryloylglycine (IAG, derived from indolylacrylic acid and present in human urine). The structure was unequivocally confirmed through comparison between the selected reaction monitoring chromatograms obtained from the urinary species and the condensation product qualitatively synthesised in the laboratory. Owing to the large amounts of both PBG and IAG in urine of AIP patients, the possible ex vivo formation of PBG-IAG in urine samples was evaluated. The product was spontaneously formed at room temperature, at 4 °C and even during storage at −20 °C when spiking a control sample with PBG. A positive correlation was found between PBG and PBG-IAG in samples collected from AIP patients. However, no correlation was found between PBG-IAG and IAG. Purified PBG-IAG did not form the characteristic chromogen after application of p-dimethylaminobenzaldehyde in HCl, thus suggesting that the current techniques used to measure PBG in urine of AIP patients based on Ehlrich's reaction do not detect this newly characterised PBG-IAG fraction.ca_CA
dc.description.sponsorShipThis work was supported by grants from Instituto de Salud Carlos III FEDER, (CP/10/00576), the Spanish ‘Fondo de Investigación Sanitaria’ (PI11/00767) to Jordi To-Figueras and from the Generalitat de Catalunya (2014 SGR 692). Technical support of Nuria Renau and mass spectrometric discussions with Juan V. Sancho are acknowledged.ca_CA
dc.format.extent8 p.ca_CA
dc.format.mimetypeapplication/pdfca_CA
dc.language.isoengca_CA
dc.publisherWileyca_CA
dc.relation.isPartOfJournal of Mass Spectrometry Volume 50, Issue 7, July 2015ca_CA
dc.rightsCopyright © 2015 John Wiley & Sons, Ltd.ca_CA
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/*
dc.subjectmass spectrometryca_CA
dc.subjecturineca_CA
dc.subjectacute intermittent porphyriaca_CA
dc.subjectporphobilinogenca_CA
dc.subjectindolyl-3-acryloylglycineca_CA
dc.titleMass spectrometric characterisation of a condensation product between porphobilinogen and indolyl-3-acryloylglycine in urine of patients with acute intermittent porphyriaca_CA
dc.typeinfo:eu-repo/semantics/articleca_CA
dc.identifier.doihttp://dx.doi.org/10.1002/jms.3603
dc.rights.accessRightsinfo:eu-repo/semantics/restrictedAccessca_CA
dc.relation.publisherVersionhttp://onlinelibrary.wiley.com/doi/10.1002/jms.3603/fullca_CA
dc.type.versioninfo:eu-repo/semantics/publishedVersionca_CA


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