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Microscale sample deposition onto hydrophobic target plates for trace level detection of neuropeptides in brain tissue by MALDI-MS

dc.contributor.authorWei, Huien_US
dc.contributor.authorDean, Stacey L.en_US
dc.contributor.authorParkin, Mark C.en_US
dc.contributor.authorNolkrantz, Kerstinen_US
dc.contributor.authorO'Callaghan, James P.en_US
dc.contributor.authorKennedy, Robert T.en_US
dc.date.accessioned2006-12-07T16:52:55Z
dc.date.available2006-12-07T16:52:55Z
dc.date.issued2005-10en_US
dc.identifier.citationWei, Hui; Dean, Stacey L.; Parkin, Mark C.; Nolkrantz, Kerstin; O'Callaghan, James P.; Kennedy, Robert T. (2005)."Microscale sample deposition onto hydrophobic target plates for trace level detection of neuropeptides in brain tissue by MALDI-MS." Journal of Mass Spectrometry 40(10): 1338-1346. <http://hdl.handle.net/2027.42/48772>en_US
dc.identifier.issn1076-5174en_US
dc.identifier.issn1096-9888en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/48772
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=16217843&dopt=citationen_US
dc.description.abstractA sample preparation method that combines a modified target plate with a nanoscale reversed-phase column (nanocolumn) was developed for detection of neuropeptides by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS). A gold-coated MALDI plate was modified with an octadecanethiol (ODT) self-assembled monolayer to create a hydrophobic surface that could concentrate peptide samples into a ∼200–500-µm diameter spot. The spot sizes generated were comparable to those obtained for a substrate patterned with 200-µm hydrophilic spots on a hydrophobic substrate. The sample spots on the ODT-coated plate were 100-fold smaller than those formed on an unmodified gold plate with a 1-µl sample and generated 10 to 50 times higher mass sensitivity for peptide standards by MALDI-TOF MS. When the sample was deposited on an ODT-modified plate from a nanocolumn, the detection limit for peptides was as low as 20 pM for 5-µl samples corresponding to 80 amol deposited. This technique was used to analyze extracts of microwave-fixed tissue from rat brain striatum. Ninety-eight putative peptides were detected including several that had masses matching neuropeptides expected in this brain region such as substance P, rimorphin, and neurotensin. Twenty-three peptides had masses that matched peaks detected by capillary liquid chromatography with electrospray ionization MS. 1 2 Copyright © 2005 John Wiley & Sons, Ltd.en_US
dc.format.extent564697 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherJohn Wiley & Sons, Ltd.en_US
dc.subject.otherChemistryen_US
dc.subject.otherAnalytical Chemistry and Spectroscopyen_US
dc.titleMicroscale sample deposition onto hydrophobic target plates for trace level detection of neuropeptides in brain tissue by MALDI-MSen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, Ann Arbor, MI, 48109, USAen_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, Ann Arbor, MI, 48109, USAen_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, Ann Arbor, MI, 48109, USAen_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, Ann Arbor, MI, 48109, USAen_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, Ann Arbor, MI, 48109, USA ; Department of Pharmacology, University of Michigan, Ann Arbor, MI, 48109, USA ; Department of Chemistry, University of Michigan, 930 North University Avenue, Ann Arbor, MI 48109-1055, USA.en_US
dc.contributor.affiliationotherHELD/TMBB, Centers for Disease Control and Prevention, Morgantown, West Virginia 26505, USAen_US
dc.identifier.pmid16217843en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/48772/1/916_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/jms.916en_US
dc.identifier.sourceJournal of Mass Spectrometryen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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