Source:http://linkedlifedata.com/resource/pubmed/id/19648027
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
10
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pubmed:dateCreated |
2009-9-22
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pubmed:abstractText |
Infrared multiple photon dissociation (IRMPD) spectroscopy was used to study formation of b2+ from nicotinyl-glycine-glycine-methyl ester (NicGGOMe). IRMPD shows that NicGGOMe is protonated at the pyridine ring of the nicotinyl group, and more importantly, that b2+ from NicGGOMe is not protonated at the oxazolone ring, as would be expected if the species were generated on the conventional bn+/yn+ oxazolone pathway, but at the pyridine ring instead. IRMPD data support a hypothesis that formation of b2+ from NicGGOMe involves mobilization and transfer of an amide position proton during the fragmentation reaction.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1879-1123
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
20
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1841-5
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pubmed:meshHeading |
pubmed-meshheading:19648027-Amides,
pubmed-meshheading:19648027-Glycine,
pubmed-meshheading:19648027-Mass Spectrometry,
pubmed-meshheading:19648027-Models, Chemical,
pubmed-meshheading:19648027-Models, Molecular,
pubmed-meshheading:19648027-Niacin,
pubmed-meshheading:19648027-Peptides,
pubmed-meshheading:19648027-Protons,
pubmed-meshheading:19648027-Spectrophotometry, Infrared
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pubmed:year |
2009
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pubmed:articleTitle |
Spectroscopic evidence for mobilization of amide position protons during CID of model peptide ions.
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pubmed:affiliation |
Department of Chemistry, Wichita State University, Wichita, Kansas 67260-0051, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't
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