Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/21602
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dc.contributor.authorWilm, M.en
dc.contributor.authorShevchenko, A.en
dc.contributor.authorHouthaeve, T.en
dc.contributor.authorBreit, S.en
dc.contributor.authorSchweigerer, L.en
dc.contributor.authorFotsis, T.en
dc.contributor.authorMann, M.en
dc.date.accessioned2015-11-24T19:16:01Z-
dc.date.available2015-11-24T19:16:01Z-
dc.identifier.issn0028-0836-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/21602-
dc.rightsDefault Licence-
dc.subjectAmino Acid Sequenceen
dc.subjectBase Sequenceen
dc.subjectCloning, Molecularen
dc.subjectDnaen
dc.subject*Electrophoresis, Polyacrylamide Gelen
dc.subjectEndothelium, Vascular/cytology/drug effectsen
dc.subjectGrowth Inhibitors/chemistry/pharmacologyen
dc.subjectHumansen
dc.subject*Mass Spectrometryen
dc.subjectMolecular Sequence Dataen
dc.subjectProteins/*chemistryen
dc.subjectRNA-Binding Proteins/chemistryen
dc.subjectSequence Analysis/*methodsen
dc.subjectSerum Albumin, Bovineen
dc.subjectTumor Cells, Cultureden
dc.titleFemtomole sequencing of proteins from polyacrylamide gels by nano-electrospray mass spectrometryen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primary10.1038/379466a0-
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/8559255-
heal.identifier.secondaryhttp://www.nature.com/nature/journal/v379/n6564/abs/379466a0.html-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.publicationDate1996-
heal.abstractMolecular analysis of complex biological structures and processes increasingly requires sensitive methods for protein sequencing. Electrospray mass spectrometry has been applied to the high-sensitivity sequencing of short peptides, but technical difficulties have prevented similar success with gel-isolated proteins. Here we report a simple and robust technique for the sequencing of proteins isolated by polyacrylamide gel electrophoresis, using nano-electrospray tandem mass spectrometry. As little as 5 ng protein starting material on Coomassie- or silver-stained gels can be sequenced. Multiple-sequence stretches of up to 16 amino acids are obtained, which identify the protein unambiguously if already present in databases or provide information to clone the corresponding gene. We have applied this method to the sequencing and cloning of a protein which inhibits the proliferation of capillary endothelial cells in vitro and thus may have potential antiangiogenic effects on solid tumours.en
heal.journalNameNatureen
heal.journalTypepeer-reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) - ΙΑΤ

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