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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/129120
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dc.contributor.authorGu, Haiwei-
dc.contributor.authorDu, Jianhai-
dc.contributor.authorCarnevale Neto, Fausto-
dc.contributor.authorCarroll, Patrick A.-
dc.contributor.authorTurner, Sally J.-
dc.contributor.authorChiorean, E. Gabriela-
dc.contributor.authorEisenmane, Robert N.-
dc.contributor.authorRaftery, Daniel-
dc.date.accessioned2015-10-21T20:24:18Z-
dc.date.accessioned2016-10-25T21:08:24Z-
dc.date.available2015-10-21T20:24:18Z-
dc.date.available2016-10-25T21:08:24Z-
dc.date.issued2015-01-01-
dc.identifierhttp://pubs.rsc.org/en/Content/ArticleLanding/2015/AN/C4AN02386B#!divAbstract-
dc.identifier.citationAnalyst. Cambridge: Royal Soc Chemistry, v. 140, n. 8, p. 2726-2734, 2015.-
dc.identifier.issn0003-2654-
dc.identifier.urihttp://hdl.handle.net/11449/129120-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/129120-
dc.description.abstractAmino acids play essential roles in both metabolism and the proteome. Many studies have profiled free amino acids (FAAs) or proteins; however, few have connected the measurement of FAA with individual amino acids in the proteome. In this study, we developed a metabolomics method to comprehensively analyze amino acids in different domains, using two examples of different sample types and disease models. We first examined the responses of FAAs and insoluble-proteome amino acids (IPAAs) to the Myc oncogene in Tet21N human neuroblastoma cells. The metabolic and proteomic amino acid profiles were quite different, even under the same Myc condition, and their combination provided a better understanding of the biological status. In addition, amino acids were measured in 3 domains (FAAs, free and soluble-proteome amino acids (FSPAAs), and IPAAs) to study changes in serum amino acid profiles related to colon cancer. A penalized logistic regression model based on the amino acids from the three domains had better sensitivity and specificity than that from each individual domain. To the best of our knowledge, this is the first study to perform a combined analysis of amino acids in different domains, and indicates the useful biological information available from a metabolomics analysis of the protein pellet. This study lays the foundation for further quantitative tracking of the distribution of amino acids in different domains, with opportunities for better diagnosis and mechanistic studies of various diseases.en
dc.description.sponsorshipInstitute of Translational Health Sciences (ITHS)-
dc.description.sponsorshipCancer Care Engineering Project at Purdue University (Department of Defense, USAMRMC)-
dc.description.sponsorshipChromosome Metabolism and Cancer Training grant-
dc.description.sponsorshipChinese National Instrumentation Program-
dc.description.sponsorshipNational Natural Science Foundation of China-
dc.description.sponsorshipCancer Care Engineering Project at Purdue University (Walther Cancer Foundation)-
dc.description.sponsorshipCancer Care Engineering Project at Purdue University (Regenstrief Foundation)-
dc.format.extent2726-2734-
dc.language.isoeng-
dc.publisherRoyal Soc Chemistry-
dc.sourceWeb of Science-
dc.titleMetabolomics method to comprehensively analyze amino acids in different domainsen
dc.typeoutro-
dc.contributor.institutionUniversity of Washington-
dc.contributor.institutionEast China Institute of Technology-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionFred Hutchinson Cancer Research Center-
dc.contributor.institutionIndiana University-
dc.description.affiliationUniversity of Washington, Department of Anesthesiology and Pain Medicine-
dc.description.affiliationUniversity of Washington, Department of Biochemistry-
dc.description.affiliationUniversity of Washington, Department of Medicine-
dc.description.affiliationEast China Institute of Technology, Jiangxi Key Laboratory for Mass Spectrometry and Instrumentation-
dc.description.affiliationFred Hutchinson Cancer Research Center, Division os Basic Sciences-
dc.description.affiliationFred Hutchinson Cancer Research Center, Public Health Sciences Division-
dc.description.affiliationUnespUniversidade Estadual Paulista, Departamento de Química Orgânica, Instituto de Química de Araraquara-
dc.description.sponsorshipIdITHS: 2R01GM085291-
dc.description.sponsorshipIdITHS: RO1 CA57138-
dc.description.sponsorshipId(Department of Defense, USAMRMC: W81XWH-08-1-0065-
dc.description.sponsorshipIdDepartment of Defense, USAMRMC: W81XWH-10-1-0540-
dc.description.sponsorshipIdChromosome Metabolism and Cancer Training grant: T32 CA009657-
dc.description.sponsorshipIdChinese National Instrumentation Program: 2011YQ170067-
dc.description.sponsorshipIdNational Natural Science Foundation of China: 21365001-
dc.identifier.doihttp://dx.doi.org/10.1039/c4an02386b-
dc.identifier.wosWOS:000352141800024-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofAnalyst-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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